Mitochondrial DNA Depletion Syndrome, Myopathic Form MeSH Supplementary Concept Data 2025

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MeSH Supplementary: Mitochondrial DNA Depletion Syndrome, Myopathic Form
Unique ID: C563698
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563698
Entry Term(s): Mitochondrial DNA Depletion Myopathy, Autosomal Recessive
Registry Numbers: 0
Heading Mapped to: *Muscular Diseases; *Mitochondrial Diseases
Frequency: 10
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Mitochondrial DNA Depletion Syndrome, Myopathic Form Preferred

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