Genetic Dilated Cardiomyopathy Due to TTN Variants Without Known Familial Disease

Circ Genom Precis Med. 2020 Dec;13(6):e003082. doi: 10.1161/CIRCGEN.120.003082. Epub 2020 Nov 15.

Authors

Emily E Brown¹, Brittney Murray¹, Joban Vaishnav¹, Emmanouil Tampakakis¹, Lili A Barouch¹, Cynthia James¹, Anne M Murphy², Daniel P Judge^{1

3}

Affiliations

¹ Division of Cardiology (E.E.B., B.M., J.V., E.T., L.A.B., C.J., D.P.J.), Johns Hopkins University, Baltimore, MD.
² Division of Pediatric Cardiology (A.M.M.), Johns Hopkins University, Baltimore, MD.
³ Division of Cardiology, Medical University of South Carolina (D.P.J.).

No abstract available

Keywords: cardiomyopathy, dilated; coronary artery disease; genetic testing; heart disease; patients.

Publication types

Letter

MeSH terms

Adolescent
Adult
Cardiomyopathy, Dilated / genetics*
Connectin / genetics*
Family
Female
Humans
Male
Middle Aged
Mutation / genetics*

Substances

Connectin
TTN protein, human

Grant support

K08 HL145135/HL/NHLBI NIH HHS/United States