Mutations in the cardiac troponin T gene show various prognoses in Japanese patients with hypertrophic cardiomyopathy

Hypertrophic cardiomyopathy (HCM) is an autosomal dominant disorder resulting from mutations in genes for at least 15 various sarcomere-related proteins including cardiac β-myosin heavy chain, cardiac myosin-binding protein C, and cardiac troponin T. The troponin T gene (TNNT2) mutation has the thir...

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Detalles Bibliográficos
Autores principales: Fujita, Etsuko, Nakanishi, Toshio, Nishizawa, Tsutomu, Hagiwara, Nobuhisa, Matsuoka, Rumiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Japan 2013
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3830204/
https://www.ncbi.nlm.nih.gov/pubmed/23494605
http://dx.doi.org/10.1007/s00380-013-0332-3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3830204/
https://www.ncbi.nlm.nih.gov/pubmed/23494605
http://dx.doi.org/10.1007/s00380-013-0332-3

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