MeSH Browser

MeSH Supplementary: NYX protein, human
Unique ID: C416505
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C416505
Entry Term(s): congenital stationary night blindness-1 protein, human; nyctalopin protein, human
Registry Number: 0
Heading Mapped to: *Proteoglycans
Frequency: 41
Note: RefSeq NM_022567
Source: Nat Genet 2000 Nov;26(3):319-23
Date of Entry: 2000/12/05
Revision Date: 2006/06/26

NYX protein, human MeSH Supplementary Concept Data 2024