MeSH Browser

MeSH Supplementary: OPA1 protein, human
Unique ID: C415198
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C415198
Entry Term(s): optic atrophy 1 (autosomal dominant) protein, human; optic atrophy 1 protein, human
Registry Numbers: EC 3.6.1.-
Heading Mapped to: *GTP Phosphohydrolases
Frequency: 477
Note: RefSeq NM_130837
Source: Nat Genet 2000 Oct;26(2):211-5
Date of Entry: 2000/11/04
Revision Date: 2006/06/26

OPA1 protein, human MeSH Supplementary Concept Data 2025