A Novel Homozygous Intronic Variant in TNNT2 Associates With Feline Cardiomyopathy

BACKGROUND: Hypertrophic 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 ho...

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Detalles Bibliográficos
Autores principales: McNamara, James W., Schuckman, Maggie, Becker, Richard C., Sadayappan, Sakthivel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Physiology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7701303/
https://www.ncbi.nlm.nih.gov/pubmed/33304277
http://dx.doi.org/10.3389/fphys.2020.608473

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7701303/
https://www.ncbi.nlm.nih.gov/pubmed/33304277
http://dx.doi.org/10.3389/fphys.2020.608473

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