In vivo co-localisation of MBNL protein with DMPK expanded-repeat transcripts

Myotonic dystrophy (DM1) is the most common form of adult muscular dystrophy and is inherited as an autosomal dominant trait. The genetic basis of DM1 is the expansion of a CTG repeat in the 3′ untranslated region of a protein kinase gene (DMPK). The molecular mechanism by which this expanded repeat...

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Detalles Bibliográficos

Publicado en:	Nucleic Acids Res
Autores principales:	Fardaei, Majid, Larkin, Ken, Brook, J. David, Hamshere, Marion G.
Formato:	Artigo
Lenguaje:	Inglês
Publicado:	Oxford University Press 2001
Materias:	Article
Acceso en línea:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC55763/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/11433021/ https://ncbi.nlm.nih.govhttps://doi.org/10.1093/nar/29.13.2766
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