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

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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Bibliographic Details
Main Authors: Valerio Caputo, Domenica Megalizzi, Carlo Fabrizio, Andrea Termine, Luca Colantoni, Carlo Caltagirone, Emiliano Giardina, Raffaella Cascella, Claudia Strafella
Format: Article
Language:English
Published: MDPI AG 2022-08-01
Series:Cells
Subjects:
FSHD
<i>DUX4</i>
muscular distrophy
genomics
transcriptomics
(epi)genetics
Online Access:https://www.mdpi.com/2073-4409/11/17/2687

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https://www.mdpi.com/2073-4409/11/17/2687

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