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Article

Facioscapulohumeral muscular dystrophy: molecular pathological advances and future directions.

Current opinion in neurology - 1 Oct 2011

Statland Jeffrey M, Tawil Rabi

Abstract excerpt

PURPOSE OF REVIEW: Recent advances have provided a model for understanding the underlying molecular genetic changes in facioscapulohumeral muscular dystrophy (FSHD). This review will highlight our current understanding and future research directions. RECENT FINDINGS: FSHD typically results from c...

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Topics

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Share to Gene Silencing
Share to Cardiomyopathy and Myosin Studies
Share to Chromosomes, Human, Pair 4

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Gene Expression Regulation

Share to Homeodomain Proteins

Share to Muscle Physiology and Disorders

Share to Muscular Dystrophy, Facioscapulohumeral

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Source

Identifiers

PMID: 21734574
DOI: 10.1097/WCO.0b013e32834959af

Genes

DUX4

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-21734574-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

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

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