MeSH Browser

MeSH Supplementary: Leigh Syndrome Due To Mitochondrial Complex I Deficiency
Unique ID: C564021
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C564021
Entry Term(s): Atpase Deficiency, Nuclear-Encoded
Registry Number: 0
Heading Mapped to: *Leigh Disease
Frequency: 4
Date of Entry: 2012/11/05
Revision Date: 2012/11/16

Leigh Syndrome Due To Mitochondrial Complex I Deficiency MeSH Supplementary Concept Data 2024