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NYX protein, human MeSH Supplementary Concept Data 2025


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 Numbers
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 Preferred
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