A Novel Homozygous Intronic Variant in TNNT2 Associates With Feline Cardiomyopathy

BackgroundHypertrophic cardiomyopathy (HCM) is a genetic disease of the heart and the most common cause of sudden cardiac death in the young. HCM is considered a disease of the sarcomere owing to the large number of mutations in genes encoding sarcomeric proteins. The riddle lies in discovering how...

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Autores principales: James W. McNamara, Maggie Schuckman, Richard C. Becker, Sakthivel Sadayappan
Formato: Artigo
Lenguaje:Inglês
Publicado: Frontiers Media S.A. 2020-11-01
Colección:Frontiers in Physiology
Materias:
Hypertrophic Cardiomyopathy
Maine Coon
MYBPC3
TNNT2
sarcomere
Acceso en línea:https://www.frontiersin.org/articles/10.3389/fphys.2020.608473/full
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