https://www.selleckchem.com/pr....oducts/ro-20-1724.ht
1 locus. This gene encodes a taurine transporter whose involvement in myocardial dysfunction and DCM is supported by numerous observations in humans and animals. At the 22q11.23 locus, in silico and data mining annotations, and to a lesser extent functional analysis, strongly suggest SMARCB1 as the candidate culprit gene. This study provides a better understanding of the genetic architecture of DCM and sheds light on novel biological pathways underlying heart failure. This study provides a better understanding of the genetic architec
Like
Comment
Share
