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Article

Myofibrillar myopathy due to dominant LMNA mutations: A report of 2 cases.

Muscle & nerve - 1 May 2018

Dhawan Priya S, Liewluck Teerin, Knapik Joseph, Milone Margherita

Abstract excerpt

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Topics

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Share to LMNA gene
Share to Lamin Type A
Share to Muscle, Skeletal
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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Myopathies, Structural, Congenital

Source

Identifiers

PMID: 29211919
DOI: 10.1002/mus.26036

Genes

LMNA

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

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Research trail→

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Myofibrillar myopathy due to dominant LMNA mutations: A report of 2 cases.PMID 29211919Read ↗

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Myofibrillar myopathies: new developments.Semantic proximity Read ↗

LAMA2-related myopathy: Frequency among congenital and limb-girdle muscular dystrophies.Semantic proximity Read ↗

A Single mtDNA Deletion in Association with a LMNA Gene New Frameshift Variant: A Case Report.Semantic proximity Read ↗

De novo LMNA mutations cause a new form of congenital muscular dystrophy.Semantic proximity Read ↗

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The most severe form of LMNA-associated congenital muscular dystrophy.Semantic proximity Read ↗

[Recent advances in LMNA gene related muscular dystrophy].Semantic proximity Read ↗

Muscle fiber type disproportion (FTD) in a family with mutations in the LMNA gene.Semantic proximity Read ↗

Germinal mosaicism for LMNA mimics autosomal recessive congenital muscular dystrophy.Semantic proximity Read ↗

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