Myasthenic Syndrome due to Mutation in SCN4A MeSH Supplementary Concept Data 2024

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Concepts

MeSH Supplementary: Myasthenic Syndrome due to Mutation in SCN4A
Unique ID: C565830
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C565830
Registry Number: 0
Heading Mapped to: *Myasthenic Syndromes, Congenital
Frequency: 0
Note: mutation iun SCN4A
Date of Entry: 2012/11/05

Myasthenic Syndrome due to Mutation in SCN4A Preferred

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