MeSH Browser

MeSH Supplementary: PEX16 protein, human
Unique ID: C486345
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C486345
Entry Term(s): peroxisomal biogenesis factor 16 protein, human
Registry Numbers: 0
Heading Mapped to: *Membrane Proteins
Frequency: 32
Note: human PeX16 is mutated in patients with Zellweger syndrome; RefSeq NM_057174
Date of Entry: 2004/08/06
Revision Date: 2006/04/17

PEX16 protein, human MeSH Supplementary Concept Data 2025