MeSH Browser

MeSH Supplementary: Mitochondrial Dna Depletion Syndrome, Encephalomyopathic Form, With Methylmalonic Aciduria, Autosomal Recessive
Unique ID: C567624
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C567624
Registry Number: 0
Heading Mapped to: *Metabolism, Inborn Errors; *Mitochondrial Myopathies
Frequency: 2
Note: mutations in SUCLA2
Date of Entry: 2012/11/05

Mitochondrial Dna Depletion Syndrome, Encephalomyopathic Form, With Methylmalonic Aciduria, Autosomal Recessive MeSH Supplementary Concept Data 2023