A novel PRRX1 loss-of-function variation contributing to familial atrial fibrillation and congenital patent ductus arteriosus

Overview of attention for article published in Genetics and Molecular Biology, January 2022

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A novel PRRX1 loss-of-function variation contributing to familial atrial fibrillation and congenital patent ductus arteriosus

Doc Wire News, 04 Apr 2022

This article was originally published here Genet Mol Biol. 2022 Mar 30;45(2):e20210378.

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