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Nemaline Myopathy 2 MeSH Supplementary Concept Data 2024


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 Number
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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