Myasthenic Syndrome, Congenital, Fast-Channel MeSH Supplementary Concept Data 2025

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Concepts

MeSH Supplementary: Myasthenic Syndrome, Congenital, Fast-Channel
Unique ID: C563832
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563832
Registry Numbers: 0
Heading Mapped to: *Myasthenic Syndromes, Congenital
Frequency: 0
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Myasthenic Syndrome, Congenital, Fast-Channel Preferred

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