RNA metabolism in myotonic dystrophy: patient muscle shows decreased insulin receptor RNA and protein consistent with abnormal insulin resistance.

Myotonic dystrophy is a dominantly inherited clinically variable multisystemic disorder, and has been found to be caused by heterozygosity for a trinucleotide repeat expansion mutation in the 3' untranslated region of a protein kinase gene (DM kinase). The mechanisms by which the expanded repea...

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Detalles Bibliográficos
Publicado en:J Clin Invest
Autores principales: Morrone, A, Pegoraro, E, Angelini, C, Zammarchi, E, Marconi, G, Hoffman, E P
Formato: Artigo
Lenguaje:Inglês
Publicado: American Society for Clinical Investigation 1997
Materias:
Research Article
Acceso en línea:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC507989/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/9120013/
https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI119332
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