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


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
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