MeSH Browser

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

Mitochondrial DNA Depletion Syndrome, Hepatocerebral Form, Autosomal Recessive MeSH Supplementary Concept Data 2025