A truncated cardiac troponin T molecule in transgenic mice suggests multiple cellular mechanisms for familial hypertrophic cardiomyopathy.

Mutations in multiple cardiac sarcomeric proteins including myosin heavy chain (MyHC) and cardiac troponin T (cTnT) cause a dominant genetic heart disease, familial hypertrophic cardiomyopathy (FHC). Patients with mutations in these two genes have quite distinct clinical characteristics. Those with...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Tardiff, J C, Factor, S M, Tompkins, B D, Hewett, T E, Palmer, B M, Moore, R L, Schwartz, S, Robbins, J, Leinwand, L A
Formato: Artigo
Idioma:Inglês
Publicado em: 1998
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC508871/
https://ncbi.nlm.nih.gov/pubmed/9637714
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados