Meeting report: the 2021 FSHD International Research Congress

Facioscapulohumeral muscular dystrophy (FSHD) is the second most common genetic myopathy, characterized by slowly progressing and highly heterogeneous muscle wasting with a typical onset in the late teens/early adulthood [1]. Although the etiology of the disease for both FSHD type 1 and type 2 has b...

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Detalles Bibliográficos
Autores principales: Jagannathan, Sujatha, de Greef, Jessica C., Hayward, Lawrence J., Yokomori, Kyoko, Gabellini, Davide, Mul, Karlien, Sacconi, Sabrina, Arjomand, Jamshid, Kinoshita, June, Harper, Scott Q.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8762812/
https://www.ncbi.nlm.nih.gov/pubmed/35039091
http://dx.doi.org/10.1186/s13395-022-00287-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8762812/
https://www.ncbi.nlm.nih.gov/pubmed/35039091
http://dx.doi.org/10.1186/s13395-022-00287-8

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