Molecular basis of Wiskott-Aldrich syndrome in patients from India
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Veröffentlicht in: | European journal of haematology 2012-10, Vol.89 (4), p.356-360 |
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container_title | European journal of haematology |
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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 |
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doi_str_mv | 10.1111/j.1600-0609.2012.01818.x |
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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 & 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 ; 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language | eng |
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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 |
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