Cargando…

Does DNA Methylation Matter in FSHD?

Facioscapulohumeral muscular dystrophy (FSHD) has been associated with the genetic and epigenetic molecular features of the CpG-rich D4Z4 repeat tandem array at 4q35. Reduced DNA methylation of D4Z4 repeats is considered part of the FSHD mechanism and has been proposed as a reliable marker in the FS...

Descripción completa

Detalles Bibliográficos
Autores principales: Salsi, Valentina, Magdinier, Frédérique, Tupler, Rossella
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7140823/
https://www.ncbi.nlm.nih.gov/pubmed/32121044
http://dx.doi.org/10.3390/genes11030258