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A founder truncating variant in GDF1 causes autosomal‐recessive right isomerism and associated congenital heart defects in multiplex Arab kindreds.

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Title: A founder truncating variant in GDF1 causes autosomal‐recessive right isomerism and associated congenital heart defects in multiplex Arab kindreds.
Authors: Marek‐Yagel, Dina1,2, Bolkier, Yoav2,3, Barel, Ortal4, Vardi, Amir2,5, Mishali, David2,5, Katz, Uriel2,3, Salem, Yishay2,3, Abudi, Shachar1,2, Nayshool, Omri4, Kol, Nitzan4, Raas‐Rothschild, Annick2,6, Rechavi, Gideon2,4,7, Anikster, Yair1,2,7, Pode‐Shakked, Ben1,2,8, ben_pode@hotmail.com
Source: American Journal of Medical Genetics. Part A; May2020, Vol. 182 Issue 5, p987-993, 7p
Database: Applied Science & Technology Source
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Header DbId: aci
DbLabel: Applied Science & Technology Source
An: 142767207
AccessLevel: 2
PubType: Academic Journal
PubTypeId: academicJournal
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  Data: A founder truncating variant in GDF1 causes autosomal‐recessive right isomerism and associated congenital heart defects in multiplex Arab kindreds.
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  Data: <searchLink fieldCode="JN" term="%22American+Journal+of+Medical+Genetics%2E+Part+A%22">American Journal of Medical Genetics. Part A</searchLink>; May2020, Vol. 182 Issue 5, p987-993, 7p
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=aci&AN=142767207
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        Value: 10.1002/ajmg.a.61509
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      – Code: eng
        Text: English
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        PageCount: 7
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      – TitleFull: A founder truncating variant in GDF1 causes autosomal‐recessive right isomerism and associated congenital heart defects in multiplex Arab kindreds.
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              M: 05
              Text: May2020
              Type: published
              Y: 2020
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