The Lebanese allele at the LDLR in normocholesterolemic people merits reconsideration of genotype phenotype correlations in familial hypercholesterolemia
Gespeichert in:
Veröffentlicht in: | Endocrine 2012-10, Vol.42 (2), p.445-448 |
---|---|
Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 448 |
---|---|
container_issue | 2 |
container_start_page | 445 |
container_title | Endocrine |
container_volume | 42 |
creator | Fahed, Akl C. Bitar, Fadi F. Khalaf, Ruby I. Moubarak, Elie M. Azar, Sami T. Nemer, Georges M. |
description | |
doi_str_mv | 10.1007/s12020-012-9669-0 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1074775710</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1074775710</sourcerecordid><originalsourceid>FETCH-LOGICAL-c344t-84984b04a1edc00ac9c024c0f52b6a75c0f40c70f57eb226a3d2dc94409b92f3</originalsourceid><addsrcrecordid>eNp9kbFu2zAQhokiRZ2kfYAuAccsao80ZVpj4KRtAAMFCg_dCIo62TQoUSHlwY-St-2pjgNkyXQ_eR__w_Fn7KuAbwJAf89CgoQChCyqxaIq4AO7FGVJgtoXpOdlWQAs_87YVc57ACnlQn9iMynVUldKX7LnzQ75GmvbY0ZuQ8BAZeTjdH2__sN9z_uYuuh2MWAeMVHpvOMDxoHQDpMfM0_oYp99g8mOPvY8tnyLfRyPA_Jhd1YupoThP5En49Z2Pngb-I666e0E-5l9bG3I-OWlXrPNj4fN6lex_v3zcXW3LtxcqbFYqmqpalBWYOMArKscSOWgLWW9sLokpcBpOmusaX07b2TjKqWgqivZzq_Z7cl2SPHpQPNN57PDEOhH4iEbAVppXWoBhIoT6lLMOWFrhuQ7m44EmSkQcwrEUCBmCsRMb25e7A91h83ri3MCBMgTkKnVbzGZfTyknjZ-x_UftTiaWw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1074775710</pqid></control><display><type>article</type><title>The Lebanese allele at the LDLR in normocholesterolemic people merits reconsideration of genotype phenotype correlations in familial hypercholesterolemia</title><source>MEDLINE</source><source>Springer Nature - Complete Springer Journals</source><creator>Fahed, Akl C. ; Bitar, Fadi F. ; Khalaf, Ruby I. ; Moubarak, Elie M. ; Azar, Sami T. ; Nemer, Georges M.</creator><creatorcontrib>Fahed, Akl C. ; Bitar, Fadi F. ; Khalaf, Ruby I. ; Moubarak, Elie M. ; Azar, Sami T. ; Nemer, Georges M.</creatorcontrib><identifier>ISSN: 1355-008X</identifier><identifier>EISSN: 1559-0100</identifier><identifier>DOI: 10.1007/s12020-012-9669-0</identifier><identifier>PMID: 22487947</identifier><language>eng</language><publisher>Boston: Springer US</publisher><subject>Adolescent ; Adult ; Alleles ; Child ; Cohort Studies ; Diabetes ; Endocrinology ; Exons ; Female ; Genetic Association Studies ; Heterozygote ; Homozygote ; Humanities and Social Sciences ; Humans ; Hyperlipoproteinemia Type II - blood ; Hyperlipoproteinemia Type II - genetics ; Hyperlipoproteinemia Type II - metabolism ; Internal Medicine ; Lebanon ; Lipoproteins, LDL - blood ; Male ; Medicine ; Medicine & Public Health ; multidisciplinary ; Mutation ; Pedigree ; Penetrance ; Receptors, LDL - genetics ; Receptors, LDL - metabolism ; Research Letter ; Science ; Young Adult</subject><ispartof>Endocrine, 2012-10, Vol.42 (2), p.445-448</ispartof><rights>Springer Science+Business Media, LLC 2012</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c344t-84984b04a1edc00ac9c024c0f52b6a75c0f40c70f57eb226a3d2dc94409b92f3</citedby><cites>FETCH-LOGICAL-c344t-84984b04a1edc00ac9c024c0f52b6a75c0f40c70f57eb226a3d2dc94409b92f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s12020-012-9669-0$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s12020-012-9669-0$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>314,776,780,27903,27904,41467,42536,51297</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22487947$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fahed, Akl C.</creatorcontrib><creatorcontrib>Bitar, Fadi F.</creatorcontrib><creatorcontrib>Khalaf, Ruby I.</creatorcontrib><creatorcontrib>Moubarak, Elie M.</creatorcontrib><creatorcontrib>Azar, Sami T.</creatorcontrib><creatorcontrib>Nemer, Georges M.</creatorcontrib><title>The Lebanese allele at the LDLR in normocholesterolemic people merits reconsideration of genotype phenotype correlations in familial hypercholesterolemia</title><title>Endocrine</title><addtitle>Endocrine</addtitle><addtitle>Endocrine</addtitle><subject>Adolescent</subject><subject>Adult</subject><subject>Alleles</subject><subject>Child</subject><subject>Cohort Studies</subject><subject>Diabetes</subject><subject>Endocrinology</subject><subject>Exons</subject><subject>Female</subject><subject>Genetic Association Studies</subject><subject>Heterozygote</subject><subject>Homozygote</subject><subject>Humanities and Social Sciences</subject><subject>Humans</subject><subject>Hyperlipoproteinemia Type II - blood</subject><subject>Hyperlipoproteinemia Type II - genetics</subject><subject>Hyperlipoproteinemia Type II - metabolism</subject><subject>Internal Medicine</subject><subject>Lebanon</subject><subject>Lipoproteins, LDL - blood</subject><subject>Male</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>multidisciplinary</subject><subject>Mutation</subject><subject>Pedigree</subject><subject>Penetrance</subject><subject>Receptors, LDL - genetics</subject><subject>Receptors, LDL - metabolism</subject><subject>Research Letter</subject><subject>Science</subject><subject>Young Adult</subject><issn>1355-008X</issn><issn>1559-0100</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kbFu2zAQhokiRZ2kfYAuAccsao80ZVpj4KRtAAMFCg_dCIo62TQoUSHlwY-St-2pjgNkyXQ_eR__w_Fn7KuAbwJAf89CgoQChCyqxaIq4AO7FGVJgtoXpOdlWQAs_87YVc57ACnlQn9iMynVUldKX7LnzQ75GmvbY0ZuQ8BAZeTjdH2__sN9z_uYuuh2MWAeMVHpvOMDxoHQDpMfM0_oYp99g8mOPvY8tnyLfRyPA_Jhd1YupoThP5En49Z2Pngb-I666e0E-5l9bG3I-OWlXrPNj4fN6lex_v3zcXW3LtxcqbFYqmqpalBWYOMArKscSOWgLWW9sLokpcBpOmusaX07b2TjKqWgqivZzq_Z7cl2SPHpQPNN57PDEOhH4iEbAVppXWoBhIoT6lLMOWFrhuQ7m44EmSkQcwrEUCBmCsRMb25e7A91h83ri3MCBMgTkKnVbzGZfTyknjZ-x_UftTiaWw</recordid><startdate>20121001</startdate><enddate>20121001</enddate><creator>Fahed, Akl C.</creator><creator>Bitar, Fadi F.</creator><creator>Khalaf, Ruby I.</creator><creator>Moubarak, Elie M.</creator><creator>Azar, Sami T.</creator><creator>Nemer, Georges M.</creator><general>Springer US</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20121001</creationdate><title>The Lebanese allele at the LDLR in normocholesterolemic people merits reconsideration of genotype phenotype correlations in familial hypercholesterolemia</title><author>Fahed, Akl C. ; Bitar, Fadi F. ; Khalaf, Ruby I. ; Moubarak, Elie M. ; Azar, Sami T. ; Nemer, Georges M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c344t-84984b04a1edc00ac9c024c0f52b6a75c0f40c70f57eb226a3d2dc94409b92f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Alleles</topic><topic>Child</topic><topic>Cohort Studies</topic><topic>Diabetes</topic><topic>Endocrinology</topic><topic>Exons</topic><topic>Female</topic><topic>Genetic Association Studies</topic><topic>Heterozygote</topic><topic>Homozygote</topic><topic>Humanities and Social Sciences</topic><topic>Humans</topic><topic>Hyperlipoproteinemia Type II - blood</topic><topic>Hyperlipoproteinemia Type II - genetics</topic><topic>Hyperlipoproteinemia Type II - metabolism</topic><topic>Internal Medicine</topic><topic>Lebanon</topic><topic>Lipoproteins, LDL - blood</topic><topic>Male</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>multidisciplinary</topic><topic>Mutation</topic><topic>Pedigree</topic><topic>Penetrance</topic><topic>Receptors, LDL - genetics</topic><topic>Receptors, LDL - metabolism</topic><topic>Research Letter</topic><topic>Science</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fahed, Akl C.</creatorcontrib><creatorcontrib>Bitar, Fadi F.</creatorcontrib><creatorcontrib>Khalaf, Ruby I.</creatorcontrib><creatorcontrib>Moubarak, Elie M.</creatorcontrib><creatorcontrib>Azar, Sami T.</creatorcontrib><creatorcontrib>Nemer, Georges M.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Endocrine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fahed, Akl C.</au><au>Bitar, Fadi F.</au><au>Khalaf, Ruby I.</au><au>Moubarak, Elie M.</au><au>Azar, Sami T.</au><au>Nemer, Georges M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Lebanese allele at the LDLR in normocholesterolemic people merits reconsideration of genotype phenotype correlations in familial hypercholesterolemia</atitle><jtitle>Endocrine</jtitle><stitle>Endocrine</stitle><addtitle>Endocrine</addtitle><date>2012-10-01</date><risdate>2012</risdate><volume>42</volume><issue>2</issue><spage>445</spage><epage>448</epage><pages>445-448</pages><issn>1355-008X</issn><eissn>1559-0100</eissn><cop>Boston</cop><pub>Springer US</pub><pmid>22487947</pmid><doi>10.1007/s12020-012-9669-0</doi><tpages>4</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1355-008X |
ispartof | Endocrine, 2012-10, Vol.42 (2), p.445-448 |
issn | 1355-008X 1559-0100 |
language | eng |
recordid | cdi_proquest_miscellaneous_1074775710 |
source | MEDLINE; Springer Nature - Complete Springer Journals |
subjects | Adolescent Adult Alleles Child Cohort Studies Diabetes Endocrinology Exons Female Genetic Association Studies Heterozygote Homozygote Humanities and Social Sciences Humans Hyperlipoproteinemia Type II - blood Hyperlipoproteinemia Type II - genetics Hyperlipoproteinemia Type II - metabolism Internal Medicine Lebanon Lipoproteins, LDL - blood Male Medicine Medicine & Public Health multidisciplinary Mutation Pedigree Penetrance Receptors, LDL - genetics Receptors, LDL - metabolism Research Letter Science Young Adult |
title | The Lebanese allele at the LDLR in normocholesterolemic people merits reconsideration of genotype phenotype correlations in familial hypercholesterolemia |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-27T15%3A14%3A21IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=The%20Lebanese%20allele%20at%20the%20LDLR%20in%20normocholesterolemic%20people%20merits%20reconsideration%20of%20genotype%20phenotype%20correlations%20in%20familial%20hypercholesterolemia&rft.jtitle=Endocrine&rft.au=Fahed,%20Akl%20C.&rft.date=2012-10-01&rft.volume=42&rft.issue=2&rft.spage=445&rft.epage=448&rft.pages=445-448&rft.issn=1355-008X&rft.eissn=1559-0100&rft_id=info:doi/10.1007/s12020-012-9669-0&rft_dat=%3Cproquest_cross%3E1074775710%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1074775710&rft_id=info:pmid/22487947&rfr_iscdi=true |