MESP1 loss‑of‑function mutation contributes to double outlet right ventricle.
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DOI: 10.3892/mmr.2017.6875
Abstract: Congenital heart disease (CHD) is the most common form of birth defect in humans, and remains a leading non‑infectious cause of infant mortality worldwide. An increasing number of studies have demonstrated that genetic defects serve… read more here.
Keywords: mesp1 loss; outlet right; double outlet; chd ... See more keywords