MeSH Browser

MeSH Supplementary: Peroxisome Biogenesis Disorder, Complementation Group 13
Unique ID: C566625
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C566625
Registry Numbers: 0
Heading Mapped to: *Peroxisomal Disorders
Frequency: 0
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Peroxisome Biogenesis Disorder, Complementation Group 13 MeSH Supplementary Concept Data 2025