Direct interplay between two candidate genes in FSHD muscular dystrophy

Facioscapulohumeral muscular dystrophy (FSHD) is one of the most common neuromuscular disorders. The major form of the disease (FSHD1) is linked to decrease in copy number of a 3.3-kb tandem repeated macrosatellite (D4Z4), located on chromosome 4q35. D4Z4 deletion alters chromatin structure of the l...

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Detalles Bibliográficos
Autores principales: Ferri, Giulia, Huichalaf, Claudia H., Caccia, Roberta, Gabellini, Davide
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2015
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4321439/
https://www.ncbi.nlm.nih.gov/pubmed/25326393
http://dx.doi.org/10.1093/hmg/ddu536

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4321439/
https://www.ncbi.nlm.nih.gov/pubmed/25326393
http://dx.doi.org/10.1093/hmg/ddu536

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