A carregar...

Delineation of Molecular Pathways Involved in Cardiomyopathies Caused by Troponin T Mutations

Familial hypertrophic cardiomyopathy (FHC) is associated with mild to severe cardiac problems and is the leading cause of sudden death in young people and athletes. Although the genetic basis for FHC is well-established, the molecular mechanisms that ultimately lead to cardiac dysfunction are not we...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Publicado no:Mol Cell Proteomics
Main Authors: Gilda, Jennifer E., Lai, Xianyin, Witzmann, Frank A., Gomes, Aldrin V.
Formato: Artigo
Idioma:Inglês
Publicado em: The American Society for Biochemistry and Molecular Biology 2016
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5083082/
https://ncbi.nlm.nih.gov/pubmed/27022107
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/mcp.M115.057380
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!