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Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form, Autosomal Recessive MeSH Supplementary Concept Data 2022


MeSH Supplementary
Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form, Autosomal Recessive
Unique ID
C567608
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C567608
Registry Number
0
Heading Mapped to
*Mitochondrial Myopathies
Frequency
6
Date of Entry
2012/11/05
Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form, Autosomal Recessive Preferred
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