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...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Front Neurol
Päätekijät: Nieuwenhuis, Sylvia, Okkersen, Kees, Widomska, Joanna, Blom, Paul, 't Hoen, Peter A. C., van Engelen, Baziel, Glennon, Jeffrey C.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Frontiers Media S.A. 2019
Aiheet:
Neurology
Linkit: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
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