MeSH Browser

MeSH Supplementary: OPA3 protein, human
Unique ID: C443108
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C443108
Entry Term(s): optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia) protein, human; optic atrophy 3 protein, human
Registry Numbers: 0
Heading Mapped to: *Proteins
Frequency: 36
Note: RefSeq NM_025136
Source: Am J Num Genet 2001 Dec;69(6):1218-24
Date of Entry: 2002/01/08
Revision Date: 2006/06/26

OPA3 protein, human MeSH Supplementary Concept Data 2025