Associated Papers
Proteomics screen to reveal molecular changes mediated by C722G missense mutation in CHRM2 gene.
Hou D et al.
Journal of Proteomics, 2013
Rare variant mutations identified in pediatric patients with dilated cardiomyopathy.
Rampersaud E et al.
Progress in Pediatric Cardiology, 2011
A missense mutation in the CHRM2 gene is associated with familial dilated cardiomyopathy.
Zhang L et al.
Circulation Research, 2008
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