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Article

Congenital muscular dystrophies: toward molecular therapeutic interventions.

Current neurology and neuroscience reports - 1 Mar 2010

Collins James, Bönnemann Carsten G

Abstract excerpt

Congenital muscular dystrophies (CMDs) are a clinically and genetically heterogeneous group of neuromuscular disorders that typically present at birth or in early infancy with hypotonia, weakness, and histologic evidence of a dystrophic myopathy. CMD biochemical types include various abnormalitie...

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Identifiers

PMID: 20425232
DOI: 10.1007/s11910-010-0092-8

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20425232-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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