Consequences of epigenetic derepression in facioscapulohumeral muscular dystrophy

Facioscapulohumeral muscular dystrophy (FSHD), a common hereditary myopathy, is caused either by the contraction of the D4Z4 macrosatellite repeat at the distal end of chromosome 4q to a size of 1 to 10 repeat units (FSHD1) or by mutations in D4Z4 chromatin modifiers such as Structural Maintenance o...

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Detalles Bibliográficos
Autores principales: Greco, Anna, Goossens, Remko, van Engelen, Baziel, van der Maarel, Silvère M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2020
Materias:
Invited Reviews
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7318180/
https://www.ncbi.nlm.nih.gov/pubmed/32086799
http://dx.doi.org/10.1111/cge.13726

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7318180/
https://www.ncbi.nlm.nih.gov/pubmed/32086799
http://dx.doi.org/10.1111/cge.13726

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