Implication of rare genetic variants of NODAL and ACVR1B in Congenital Heart Disease patients from Indian Population.
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DOI: 10.1016/j.yexcr.2021.112869
Abstract: NODAL signaling plays an essential role in vertebrate embryonic patterning and heart development. Accumulating evidences suggest that genetic mutations in TGF-β/NODAL signaling pathway can cause congenital heart disease in humans. To investigate the implication of… read more here.
Keywords: heart; heart disease; nodal acvr1b; congenital heart ... See more keywords