MeSH Browser

MeSH Supplementary: IMPDH1, mouse
Unique ID: C463299
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C463299
Entry Term(s): inosine monophosphate dehydrogenase 1, mouse
Registry Numbers: EC 1.1.1.205
Heading Mapped to: *IMP Dehydrogenase
Frequency: 18
Note: mutant causes the RP10 form of autosomal dominant retinitis pigmentosa in mice
Source: Hum Mol Genet 2002 Mar 1;11(5)
Date of Entry: 2002/08/16
Revision Date: 2002/08/16

IMPDH1, mouse MeSH Supplementary Concept Data 2025