Meeting report: the 2021 FSHD International Research Congress

Meeting report: the 2021 FSHD International Research Congress

Abstract 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 typ...

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Bibliographic Details
Main Authors: Sujatha Jagannathan, Jessica C. de Greef, Lawrence J. Hayward, Kyoko Yokomori, Davide Gabellini, Karlien Mul, Sabrina Sacconi, Jamshid Arjomand, June Kinoshita, Scott Q. Harper
Format: Article
Language:English
Published: BMC 2022-01-01
Series:Skeletal Muscle
Online Access:https://doi.org/10.1186/s13395-022-00287-8

Internet

https://doi.org/10.1186/s13395-022-00287-8

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