RNA/MBNL1-containing foci in myoblast nuclei from patients affected by myotonic dystrophy type 2: an immunocytochemical study

Myotonic dystrophy type 2 (DM2) is a dominantly inherited autosomal disease with multi-systemic clinical features and it is caused by expansion of a CCTG tetranucleotide repeat in the first intron of the zinc finger protein 9 (ZNF9) gene in 3q21.The expanded-CCUG-containing transcripts are retained...

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Detalhes bibliográficos
Main Authors: Perdoni, F., Malatesta, M., Cardani, R., Giagnacovo, M., Mancinelli, E., Meola, G., Pellicciari, C.
Formato: Artigo
Idioma:Inglês
Publicado em: PAGEPress Publications 2009
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Original Paper
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3168229/
https://ncbi.nlm.nih.gov/pubmed/30256871
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4081/ejh.2009.e18
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