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Article

A mutation in the α tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy

1 Jan 1995

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Share to Cardiomyopathy and Myosin Studies
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 7663526
DOI: 10.1038/ng0195-75

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Related research

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Click a neighbor to travelStep 1 · 12 closest

A mutation in the α tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathyPMID 7663526Read ↗

Identification of a founder mutation in TPM3 in nemaline myopathy patients of Turkish originSemantic proximity Read ↗

Mutations of the slow muscle α-tropomyosin gene, <i>TPM3</i> , are a rare cause of nemaline myopathySemantic proximity Read ↗

A novel variant in the tropomyosin 3 gene presenting as an adult-onset distal myopathy - a case report.Semantic proximity Read ↗

A TPM3 mutation causing cap myopathySemantic proximity Read ↗

A Novel Variant in TPM3 Causing Muscle Weakness and Concomitant Hypercontractile Phenotype.Semantic proximity Read ↗

Mutation update and genotype-phenotype correlations of novel and previously described mutations in TPM2 and TPM3 causing congenital myopathies.Semantic proximity Read ↗

Mutations in <i>TPM3</i> are a common cause of congenital fiber type disproportionSemantic proximity Read ↗

Tropomyosin 3 (TPM3) function in skeletal muscle and in myopathy.Semantic proximity Read ↗

Novel autosomal dominant TPM3 mutation causes a combined congenital fibre type disproportion-cap disease histological pattern.Semantic proximity Read ↗

A second pedigree with autosomal dominant nemaline myopathy caused by TPM3 mutation: a clinical and pathological study.Semantic proximity Read ↗

Novel mutation in the alpha-tropomyosin gene and transition from hypertrophic to hypocontractile dilated cardiomyopathy.Semantic proximity Read ↗

Mutations of tropomyosin 3 (TPM3) are common and associated with type 1 myofiber hypotrophy in congenital fiber type disproportion.Semantic proximity Read ↗

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