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

Overview of attention for article published in Frontiers in Genetics, December 2017

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RT @FrontGenetics: A Novel Role for CSRP1 in a Lebanese Family with Congenital Cardiac Defects: Amina Kamar, Akl C. Fahed, Kamel Shibbani,…

Di-genic model of inheritance for CSRP1 variant https://t.co/FMOI6T9IFb in a large #consanguineous #Labanese family with Congenital #heart defect & #polydactyly #cardiology #hearthealth #genetics https://t.co/22gO5qk1eQ

More candidate gene discovery for congenital heart disease by studying consanguineous families from the Middle East. In this family, we report digenic inheritance of CSRP1 and TRPS1 variants @nemerg @Nehme_ELHACHEM https://t.co/6iPhxvnvrG

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

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