A Novel Role for CSRP1 in a Lebanese Family with Congenital Cardiac Defects

A Novel Role for CSRP1 in a Lebanese Family with Congenital Cardiac Defects

Despite an obvious role for consanguinity in congenital heart disease (CHD), most studies fail to document a monogenic model of inheritance except for few cases. We hereby describe a first-degree cousins consanguineous Lebanese family with 7 conceived children: 2 died in utero of unknown causes, 3 h...

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Bibliographic Details
Main Authors: Amina Kamar, Akl C. Fahed, Kamel Shibbani, Nehme El-Hachem, Salim Bou-Slaiman, Mariam Arabi, Mazen Kurban, Jonathan G. Seidman, Christine E. Seidman, Rachid Haidar, Elias Baydoun, Georges Nemer, Fadi Bitar
Format: Article
Language:English
Published: Frontiers Media S.A. 2017-12-01
Series:Frontiers in Genetics
Subjects:
congenital heart disease
CSRP1
TRPS1
polydactyly
Online Access:http://journal.frontiersin.org/article/10.3389/fgene.2017.00217/full

Internet

http://journal.frontiersin.org/article/10.3389/fgene.2017.00217/full

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