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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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Bibliografski detalji
Glavni autori: Morrone, A, Pegoraro, E, Angelini, C, Zammarchi, E, Marconi, G, Hoffman, E P
Format: Artigo
Jezik:Inglês
Izdano: 1997
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC507989/
https://ncbi.nlm.nih.gov/pubmed/9120013
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