MeSH Browser

MeSH Supplementary: Nemaline myopathy 4
Unique ID: C538351
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C538351
Entry Term(s): Cap Myopathy, Tpm2-Related; Nemaline myopathy caused by mutation in the tropomyosin 2 gene
Registry Numbers: 0
Heading Mapped to: *Myopathies, Nemaline
Frequency: 2
Date of Entry: 2010/08/25
Revision Date: 2012/11/05

Nemaline myopathy 4 MeSH Supplementary Concept Data 2025