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MEF2C loss-of-function mutation contributes to congenital heart defects

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0 Published in 2017 at "International Journal of Medical Sciences"

DOI: 10.7150/ijms.21353

Abstract: Congenital heart disease (CHD) is the most common type of developmental abnormality in humans, and is a leading cause for substantially increased morbidity and mortality in affected individuals. Increasing studies demonstrates a pivotal role of… read more here.

Keywords: mef2c loss; loss function; chd; function mutation ... See more keywords