Decoding Dysfunction in Duchenne Muscular Dystrophy Cardiomyopathy

Circ Genom Precis Med. 2018 Jan;11(1):e002051. doi: 10.1161/CIRCGEN.117.002051.

Authors

Nosheen Reza¹, Anjali T Owens²

Affiliations

¹ From the Center for Inherited Cardiovascular Disease, Division of Cardiovascular Medicine, Department of Medicine, University of Pennsylvania Perelman School of Medicine, Philadelphia.
² From the Center for Inherited Cardiovascular Disease, Division of Cardiovascular Medicine, Department of Medicine, University of Pennsylvania Perelman School of Medicine, Philadelphia. anjali.owens@uphs.upenn.edu.

PMID: 29874187
DOI: 10.1161/CIRCGEN.117.002051

No abstract available

Keywords: Editorials; cardiomyopathy; dystrophin; genetics; muscular dystrophy, Duchenne.

Publication types

Editorial
Comment

MeSH terms

Cardiomyopathies
Dystrophin / genetics*
Humans
Muscular Dystrophy, Duchenne / genetics*
Mutation
Open Reading Frames

Substances

Dystrophin

Grants and funding

T32 HG009495/HG/NHGRI NIH HHS/United States