Insulin Signaling as a Key Moderator in Myotonic Dystrophy Type 1

Myotonic dystrophy type 1 (DM1) is an autosomal dominant genetic disease characterized by multi-system involvement. Affected organ system includes skeletal muscle, heart, gastro-intestinal system and the brain. In this review, we evaluate the evidence for alterations in insulin signaling and their r...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Publicado no:Front Neurol
Main Authors: Nieuwenhuis, Sylvia, Okkersen, Kees, Widomska, Joanna, Blom, Paul, 't Hoen, Peter A. C., van Engelen, Baziel, Glennon, Jeffrey C.
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2019
Assuntos:
Neurology
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6901991/
https://ncbi.nlm.nih.gov/pubmed/31849810
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fneur.2019.01229
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados