Nemaline Myopathy 2 MeSH Supplementary Concept Data 2025

Details
Concepts

MeSH Supplementary: Nemaline Myopathy 2
Unique ID: C538349
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C538349
Entry Term(s): Nemaline myopathy caused by mutation in the nebulin gene
Registry Numbers: 0
Heading Mapped to: *Myopathies, Nemaline
Frequency: 7
Date of Entry: 2010/08/25
Revision Date: 2012/11/05

Nemaline Myopathy 2 Preferred

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