Loss of FHL1 induces an age-dependent skeletal muscle myopathy associated with myofibrillar and intermyofibrillar disorganization in mice

Recent human genetic studies have provided evidences that sporadic or inherited missense mutations in four-and-a-half LIM domain protein 1 (FHL1), resulting in alterations in FHL1 protein expression, are associated with rare congenital myopathies, including reducing body myopathy and Emery–Dreifuss...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Domenighetti, Andrea A., Chu, Pao-Hsien, Wu, Tongbin, Sheikh, Farah, Gokhin, David S., Guo, Ling T., Cui, Ziyou, Peter, Angela K., Christodoulou, Danos C., Parfenov, Michael G., Gorham, Joshua M., Li, Daniel Y., Banerjee, Indroneal, Lai, Xianyin, Witzmann, Frank A., Seidman, Christine E., Seidman, Jonathan G., Gomes, Aldrin V., Shelton, G. Diane, Lieber, Richard L., Chen, Ju
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2014
Assuntos:
Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3916749/
https://ncbi.nlm.nih.gov/pubmed/23975679
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddt412
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados