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Article

[Facioscapulohumeral muscular dystrophy type 2].

Revue neurologique - 1 Jan 2000

Sacconi S, Desnuelle C

Abstract excerpt

INTRODUCTION: In recent years, the advances of knowledge in clinical, genetic and epigenetic features of facioscapulohumeral muscular dystrophy (FSHD) allowed the identification of two forms of FSHD, the classical autosomal dominant FSHD type 1, and FSHD type 2 characterized by an identical clini...

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Share to Chromosomes, Human, Pair 4
Share to Epigenesis, Genetic
Share to Genetic Predisposition to Disease

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Muscular Dystrophy, Facioscapulohumeral

Source

Identifiers

PMID: 23969240
DOI: 10.1016/j.neurol.2013.02.004

Genes

DUX4

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-23969240-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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