Myopathy, Congenital, Compton-North MeSH Supplementary Concept Data 2025

Details
Concepts

MeSH Supplementary: Myopathy, Congenital, Compton-North
Unique ID: C567261
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567261
Registry Numbers: 0
Heading Mapped to: *Myasthenic Syndromes, Congenital
Frequency: 0
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Myopathy, Congenital, Compton-North Preferred

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