Update on the Molecular Aspects and Methods Underlying the Complex Architecture of FSHD

Despite the knowledge of the main mechanisms involved in facioscapulohumeral muscular dystrophy (FSHD), the high heterogeneity and variable penetrance of the disease complicate the diagnosis, characterization and genotype–phenotype correlation of patients and families, raising the need for further r...

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Detalles Bibliográficos
Autores principales: Caputo, Valerio, Megalizzi, Domenica, Fabrizio, Carlo, Termine, Andrea, Colantoni, Luca, Caltagirone, Carlo, Giardina, Emiliano, Cascella, Raffaella, Strafella, Claudia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9454908/
https://www.ncbi.nlm.nih.gov/pubmed/36078093
http://dx.doi.org/10.3390/cells11172687

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9454908/
https://www.ncbi.nlm.nih.gov/pubmed/36078093
http://dx.doi.org/10.3390/cells11172687

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