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

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Bibliographic Details
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
Description
ISSN:15524825
DOI:10.1002/ajmg.a.61509