A Novel Mutation in FOXC1 in a Lebanese Family with Congenital Heart Disease and Anterior Segment Dysgenesis: Potential Roles for NFATC1 and DPT in the Phenotypic Variations

Overview of attention for article published in Frontiers in Cardiovascular Medicine, September 2017

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A Novel Mutation in FOXC1 in a Lebanese Family with Congenital Heart Disease and Anterior Segment Dysgenesis:… https://t.co/0b3RvAZao1

RT @FrontCVMedicine: A Novel Mutation in FOXC1 in a Lebanese Family with Congenital Heart Disease and Anterior Segment Dysgenesis:… https:/…

A Novel Mutation in FOXC1 in a Lebanese Family with Congenital Heart Disease and Anterior Segment Dysgenesis:… https://t.co/UYnB1thMva

Congratulations Georges on your newly published @FrontiersIn article: https://t.co/aqzDtGap4J

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