MeSH Browser

MeSH Supplementary: Nemaline myopathy 1
Unique ID: C538348
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C538348
Entry Term(s): Cap Myopathy, Tpm3-Related; Nemaline myopathy caused by mutation in the tropomyosin 3 gene
Registry Numbers: 0
Heading Mapped to: *Myopathies, Nemaline
Frequency: 0
Date of Entry: 2010/08/25
Revision Date: 2012/11/05

Nemaline myopathy 1 MeSH Supplementary Concept Data 2025