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Article

Lamin-Related Congenital Muscular Dystrophy Alters Mechanical Signaling and Skeletal Muscle Growth.

International journal of molecular sciences - 30 Dec 2020

Owens Daniel J, Messéant Julien, Moog Sophie, Viggars Mark, Ferry Arnaud, Mamchaoui Kamel, Lacène Emmanuelle, Roméro Norma, Brull Astrid, Bonne Gisèle, Butler-Browne Gillian, Coirault Catherine

Abstract excerpt

Laminopathies are a clinically heterogeneous group of disorders caused by mutations in the LMNA gene, which encodes the nuclear envelope proteins lamins A and C. The most frequent diseases associated with LMNA mutations are characterized by skeletal and cardiac involvement, and include autosomal dominant Emery-Dreifuss muscular dystrophy (EDMD), limb-girdle muscular dystrophy type 1B, and LMNA-related congenital...

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Identifiers

PMID: 33396724
DOI: 10.3390/ijms22010306
PMCID: PMC7795708

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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