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Article

Clinico-genetic heterogeneity in Pakistani families affected with muscular dystrophies.

Molecular biology reports - 19 Mar 2026

Ahmad Riaz, Hashmi Muhammad Almas, Ullah Asad, Rehman Ubaid Ur, Naeem Muhammad, Houlden Henry

Abstract excerpt

BACKGROUND: Muscular dystrophies are a group of inherited neuromuscular disorders characterized by degenerative and progressive muscle weakness. Duchenne muscular dystrophy (DMD), Becker muscular dystrophy (BMD) and merosin-deficient congenital muscular dystrophy type 1 (MDC1A) are frequent forms caused by DMD (NM_004006.3) and LAMA2 (NM_000426.4) mutations, respectively. METHODS AND RESULTS: Our study used whole...

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Source

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Identifiers

PMID: 41854802
DOI: 10.1007/s11033-026-11679-0
PMCID: PMC13002693

Genes

DMD
LAMA2

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 20 Oct 2026.

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