MeSH Browser

MeSH Supplementary: Myopathy due to Malate-Aspartate Shuttle Defect
Unique ID: C564973
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C564973
Registry Numbers: 0
Heading Mapped to: *Amino Acid Metabolism, Inborn Errors; *Muscular Diseases
Frequency: 0
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Myopathy due to Malate-Aspartate Shuttle Defect MeSH Supplementary Concept Data 2025