Molecular basis of Wiskott-Aldrich syndrome in patients from India

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:European journal of haematology 2012-10, Vol.89 (4), p.356-360
Hauptverfasser: David, Sachin, Jayandharan, Giridhara Rao, Abraham, Aby, Jacob, Rintu R, Devi, Govindanattar Sankari, Patkar, Nikhil, Shaji, Ramachandran V, Nair, Sukesh C, Viswabandya, Auro, Ahmed, Rayaz, George, Biju, Mathews, Vikram, Chandy, Mammen, Srivastava, Alok
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 360
container_issue 4
container_start_page 356
container_title European journal of haematology
container_volume 89
creator David, Sachin
Jayandharan, Giridhara Rao
Abraham, Aby
Jacob, Rintu R
Devi, Govindanattar Sankari
Patkar, Nikhil
Shaji, Ramachandran V
Nair, Sukesh C
Viswabandya, Auro
Ahmed, Rayaz
George, Biju
Mathews, Vikram
Chandy, Mammen
Srivastava, Alok
description
doi_str_mv 10.1111/j.1600-0609.2012.01818.x
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_proquest_miscellaneous_1039888983</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1039888983</sourcerecordid><originalsourceid>FETCH-LOGICAL-i3038-aa0aaf6d95db042525432a1c73891f881d29ebd901d105108884d4d975c1b8aa3</originalsourceid><addsrcrecordid>eNo9kEFPwzAMhSMEgjH4CyhHLi12krbJgQMgYMAYFxDHKG1SkdG1o-nE9u9pGcwXW37vWfJHCEWIsa-LeYwpQAQpqJgBshhQoozXe2S0E_bJCBSwSAiBR-Q4hDkAMIXZITliLM2UAjEi189N5YpVZVqam-ADbUr67sNn03XRVWVbX3zQsKlt2ywc9TVdms67ugu07Df0obbenJCD0lTBnf71MXm7u329mUTTl_uHm6tp5DlwGRkDxpSpVYnNQbCEJYIzg0XGpcJSSrRMudwqQIuQIEgphRVWZUmBuTSGj8n59u6ybb5WLnR64UPhqsrUrlkFjcBVH1KS99azP-sqXzirl61fmHaj___uDZdbw7ev3GanI-iBr57rAaMeMOqBr_7lq9f69nEyTH0-2uZ96Nx6lzftp04zniX6fXavp0ywp9n1RD_xH7h1e3w</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1039888983</pqid></control><display><type>article</type><title>Molecular basis of Wiskott-Aldrich syndrome in patients from India</title><source>MEDLINE</source><source>Access via Wiley Online Library</source><creator>David, Sachin ; Jayandharan, Giridhara Rao ; Abraham, Aby ; Jacob, Rintu R ; Devi, Govindanattar Sankari ; Patkar, Nikhil ; Shaji, Ramachandran V ; Nair, Sukesh C ; Viswabandya, Auro ; Ahmed, Rayaz ; George, Biju ; Mathews, Vikram ; Chandy, Mammen ; Srivastava, Alok</creator><creatorcontrib>David, Sachin ; Jayandharan, Giridhara Rao ; Abraham, Aby ; Jacob, Rintu R ; Devi, Govindanattar Sankari ; Patkar, Nikhil ; Shaji, Ramachandran V ; Nair, Sukesh C ; Viswabandya, Auro ; Ahmed, Rayaz ; George, Biju ; Mathews, Vikram ; Chandy, Mammen ; Srivastava, Alok</creatorcontrib><identifier>ISSN: 0902-4441</identifier><identifier>EISSN: 1600-0609</identifier><identifier>DOI: 10.1111/j.1600-0609.2012.01818.x</identifier><identifier>PMID: 22679904</identifier><language>eng</language><publisher>England: Blackwell Publishing Ltd</publisher><subject>Child ; Child, Preschool ; Female ; Genotype ; Humans ; India ; Infant ; Male ; Mutation ; Wiskott-Aldrich Syndrome - genetics ; Wiskott-Aldrich Syndrome - pathology</subject><ispartof>European journal of haematology, 2012-10, Vol.89 (4), p.356-360</ispartof><rights>2012 John Wiley &amp; Sons A/S</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1600-0609.2012.01818.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1600-0609.2012.01818.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>315,781,785,1418,27929,27930,45579,45580</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22679904$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>David, Sachin</creatorcontrib><creatorcontrib>Jayandharan, Giridhara Rao</creatorcontrib><creatorcontrib>Abraham, Aby</creatorcontrib><creatorcontrib>Jacob, Rintu R</creatorcontrib><creatorcontrib>Devi, Govindanattar Sankari</creatorcontrib><creatorcontrib>Patkar, Nikhil</creatorcontrib><creatorcontrib>Shaji, Ramachandran V</creatorcontrib><creatorcontrib>Nair, Sukesh C</creatorcontrib><creatorcontrib>Viswabandya, Auro</creatorcontrib><creatorcontrib>Ahmed, Rayaz</creatorcontrib><creatorcontrib>George, Biju</creatorcontrib><creatorcontrib>Mathews, Vikram</creatorcontrib><creatorcontrib>Chandy, Mammen</creatorcontrib><creatorcontrib>Srivastava, Alok</creatorcontrib><title>Molecular basis of Wiskott-Aldrich syndrome in patients from India</title><title>European journal of haematology</title><addtitle>Eur J Haematol</addtitle><subject>Child</subject><subject>Child, Preschool</subject><subject>Female</subject><subject>Genotype</subject><subject>Humans</subject><subject>India</subject><subject>Infant</subject><subject>Male</subject><subject>Mutation</subject><subject>Wiskott-Aldrich Syndrome - genetics</subject><subject>Wiskott-Aldrich Syndrome - pathology</subject><issn>0902-4441</issn><issn>1600-0609</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo9kEFPwzAMhSMEgjH4CyhHLi12krbJgQMgYMAYFxDHKG1SkdG1o-nE9u9pGcwXW37vWfJHCEWIsa-LeYwpQAQpqJgBshhQoozXe2S0E_bJCBSwSAiBR-Q4hDkAMIXZITliLM2UAjEi189N5YpVZVqam-ADbUr67sNn03XRVWVbX3zQsKlt2ywc9TVdms67ugu07Df0obbenJCD0lTBnf71MXm7u329mUTTl_uHm6tp5DlwGRkDxpSpVYnNQbCEJYIzg0XGpcJSSrRMudwqQIuQIEgphRVWZUmBuTSGj8n59u6ybb5WLnR64UPhqsrUrlkFjcBVH1KS99azP-sqXzirl61fmHaj___uDZdbw7ev3GanI-iBr57rAaMeMOqBr_7lq9f69nEyTH0-2uZ96Nx6lzftp04zniX6fXavp0ywp9n1RD_xH7h1e3w</recordid><startdate>201210</startdate><enddate>201210</enddate><creator>David, Sachin</creator><creator>Jayandharan, Giridhara Rao</creator><creator>Abraham, Aby</creator><creator>Jacob, Rintu R</creator><creator>Devi, Govindanattar Sankari</creator><creator>Patkar, Nikhil</creator><creator>Shaji, Ramachandran V</creator><creator>Nair, Sukesh C</creator><creator>Viswabandya, Auro</creator><creator>Ahmed, Rayaz</creator><creator>George, Biju</creator><creator>Mathews, Vikram</creator><creator>Chandy, Mammen</creator><creator>Srivastava, Alok</creator><general>Blackwell Publishing Ltd</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>201210</creationdate><title>Molecular basis of Wiskott-Aldrich syndrome in patients from India</title><author>David, Sachin ; Jayandharan, Giridhara Rao ; Abraham, Aby ; Jacob, Rintu R ; Devi, Govindanattar Sankari ; Patkar, Nikhil ; Shaji, Ramachandran V ; Nair, Sukesh C ; Viswabandya, Auro ; Ahmed, Rayaz ; George, Biju ; Mathews, Vikram ; Chandy, Mammen ; Srivastava, Alok</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-i3038-aa0aaf6d95db042525432a1c73891f881d29ebd901d105108884d4d975c1b8aa3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Child</topic><topic>Child, Preschool</topic><topic>Female</topic><topic>Genotype</topic><topic>Humans</topic><topic>India</topic><topic>Infant</topic><topic>Male</topic><topic>Mutation</topic><topic>Wiskott-Aldrich Syndrome - genetics</topic><topic>Wiskott-Aldrich Syndrome - pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>David, Sachin</creatorcontrib><creatorcontrib>Jayandharan, Giridhara Rao</creatorcontrib><creatorcontrib>Abraham, Aby</creatorcontrib><creatorcontrib>Jacob, Rintu R</creatorcontrib><creatorcontrib>Devi, Govindanattar Sankari</creatorcontrib><creatorcontrib>Patkar, Nikhil</creatorcontrib><creatorcontrib>Shaji, Ramachandran V</creatorcontrib><creatorcontrib>Nair, Sukesh C</creatorcontrib><creatorcontrib>Viswabandya, Auro</creatorcontrib><creatorcontrib>Ahmed, Rayaz</creatorcontrib><creatorcontrib>George, Biju</creatorcontrib><creatorcontrib>Mathews, Vikram</creatorcontrib><creatorcontrib>Chandy, Mammen</creatorcontrib><creatorcontrib>Srivastava, Alok</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>European journal of haematology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>David, Sachin</au><au>Jayandharan, Giridhara Rao</au><au>Abraham, Aby</au><au>Jacob, Rintu R</au><au>Devi, Govindanattar Sankari</au><au>Patkar, Nikhil</au><au>Shaji, Ramachandran V</au><au>Nair, Sukesh C</au><au>Viswabandya, Auro</au><au>Ahmed, Rayaz</au><au>George, Biju</au><au>Mathews, Vikram</au><au>Chandy, Mammen</au><au>Srivastava, Alok</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Molecular basis of Wiskott-Aldrich syndrome in patients from India</atitle><jtitle>European journal of haematology</jtitle><addtitle>Eur J Haematol</addtitle><date>2012-10</date><risdate>2012</risdate><volume>89</volume><issue>4</issue><spage>356</spage><epage>360</epage><pages>356-360</pages><issn>0902-4441</issn><eissn>1600-0609</eissn><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>22679904</pmid><doi>10.1111/j.1600-0609.2012.01818.x</doi><tpages>5</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0902-4441
ispartof European journal of haematology, 2012-10, Vol.89 (4), p.356-360
issn 0902-4441
1600-0609
language eng
recordid cdi_proquest_miscellaneous_1039888983
source MEDLINE; Access via Wiley Online Library
subjects Child
Child, Preschool
Female
Genotype
Humans
India
Infant
Male
Mutation
Wiskott-Aldrich Syndrome - genetics
Wiskott-Aldrich Syndrome - pathology
title Molecular basis of Wiskott-Aldrich syndrome in patients from India
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-14T00%3A52%3A15IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Molecular%20basis%20of%20Wiskott-Aldrich%20syndrome%20in%20patients%20from%20India&rft.jtitle=European%20journal%20of%20haematology&rft.au=David,%20Sachin&rft.date=2012-10&rft.volume=89&rft.issue=4&rft.spage=356&rft.epage=360&rft.pages=356-360&rft.issn=0902-4441&rft.eissn=1600-0609&rft_id=info:doi/10.1111/j.1600-0609.2012.01818.x&rft_dat=%3Cproquest_pubme%3E1039888983%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1039888983&rft_id=info:pmid/22679904&rfr_iscdi=true