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Published on: April 3, 2021
Pearls in the junk: dissecting the molecular pathogenesis of facioscapulohumeral muscular dystrophy
Petr Dmitriev1, Marc Lipinski, Yegor S Vassetzky
1Université Paris-Sud 11 CNRS UMR 8126, Interactions moléculaires et cancer, Institut de Cancérologie Gustave-Roussy, F-94805 Villejuif cedex, France.
Abstract:
Despite the discovery of the deletion on the long arm of the chromosome 4 specific for facioscapulohumeral muscular dystrophy (FSHD), the identity of the gene responsible for the disease still remains a mystery. In this review we focus on two genes, DUX4 and DUX4c, encoded by the D4Z4 repeats present in the 4q35 locus, which is affected in the disease.
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