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Article

TPM3 mutation in one of the original cases of cap disease.

Neurology - 2 Jun 2009

Ohlsson Monica, Fidzianska Anna, Tajsharghi Homa, Oldfors Anders

Abstract excerpt

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Topics

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 19487656
DOI: 10.1212/WNL.0b013e3181a82659

Genes

TPM3

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 11 closest

TPM3 mutation in one of the original cases of cap disease.PMID 19487656Read ↗

A TPM3 mutation causing cap myopathySemantic proximity Read ↗

Cap disease caused by heterozygous deletion of the β-tropomyosin gene TPM2Semantic proximity Read ↗

Noncompaction and the novel variant c.425A>T in TPM1.Semantic proximity Read ↗

ATP1A3 mutation presenting as CAPOS syndrome + dystonia phenotype.Semantic proximity Read ↗

A novel TPMT missense mutation associated with TPMT deficiency in a 5-year-old boy with ALLSemantic proximity Read ↗

Novel TPM3 mutation in a family with cap myopathy and review of the literature.Semantic proximity Read ↗

Rapp-Hodgkin and AEC syndromes due to a new frameshift mutation in the TP63 gene.Semantic proximity Read ↗

Evidence for a dominant negative disease mechanism in cap myopathy due to TPM3.Semantic proximity Read ↗

Severe progressive brain involvement in a patient with TRMT10C mutation.Semantic proximity Read ↗

A novel mutation in the TAP2 gene in bare lymphocyte syndrome: association with metastatic cutaneous squamous cell carcinoma.Semantic proximity Read ↗

Cap disease due to mutation of the beta-tropomyosin gene (TPM2).Semantic proximity Read ↗

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