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

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MeSH Supplementary: Peroxisome Biogenesis Disorder, Complementation Group G
Unique ID: C566406
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C566406
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 G Preferred

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