Thin-filament mutations, hypertrophic cardiomyopathy, and risk

J Am Coll Cardiol. 2014 Dec 23;64(24):2601-2604. doi: 10.1016/j.jacc.2014.10.007.

Authors

Mark V Sherrid¹, Milla Arabadjian², Anna Koulova²

Affiliations

¹ Hypertrophic Cardiomyopathy Program, Mount Sinai Roosevelt and St. Luke's Hospitals, Icahn School of Medicine at Mount Sinai, New York, New York. Electronic address: msherrid@chpnet.org.
² Hypertrophic Cardiomyopathy Program, Mount Sinai Roosevelt and St. Luke's Hospitals, Icahn School of Medicine at Mount Sinai, New York, New York.

PMID: 25524338
DOI: 10.1016/j.jacc.2014.10.007

No abstract available

Keywords: actins; genotype; myosin; sudden cardiac death; troponin; troponin T.

Publication types

Editorial
Comment

MeSH terms

Actins / genetics*
Cardiomyopathy, Hypertrophic*
Female
Humans
MAP Kinase Kinase Kinases / genetics*
Male
Protein Serine-Threonine Kinases
Troponin T / genetics*

Substances

ACTC1 protein, human
Actins
TNNT2 protein, human
Troponin T
Protein Serine-Threonine Kinases
TNNI3K protein, human
MAP Kinase Kinase Kinases