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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Detalles Bibliográficos
Autores principales: Perdoni, F., Malatesta, M., Cardani, R., Giagnacovo, M., Mancinelli, E., Meola, G., Pellicciari, C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PAGEPress Publications 2009
Materias:
Original Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3168229/
https://www.ncbi.nlm.nih.gov/pubmed/30256871
http://dx.doi.org/10.4081/ejh.2009.e18

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3168229/
https://www.ncbi.nlm.nih.gov/pubmed/30256871
http://dx.doi.org/10.4081/ejh.2009.e18

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