Altered Tnnt3 characterizes selective weakness of fast fibers in mice overexpressing FSHD region gene 1 (FRG1)

Facioscapulohumeral muscular dystrophy (FSHD), a common hereditary myopathy, is characterized by atrophy and weakness of selective muscle groups. FSHD is considered an autosomal dominant disease with incomplete penetrance and unpredictable variability of clinical expression within families. Mice ove...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Sancisi, Valentina, Germinario, Elena, Esposito, Alessandra, Morini, Elisabetta, Peron, Samantha, Moggio, Maurizio, Tomelleri, Giuliano, Danieli-Betto, Daniela, Tupler, Rossella
Formato: Artigo
Idioma:Inglês
Publicado em: American Physiological Society 2013
Assuntos:
Translational Physiology
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3921317/
https://ncbi.nlm.nih.gov/pubmed/24305066
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1152/ajpregu.00379.2013
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados