MeSH Browser

MeSH Supplementary: NHS protein, human
Unique ID: C488621
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C488621
Entry Term(s): Nance-Horan syndrome (congenital cataracts and dental anomalies) protein, human; Nance-Horan syndrome protein, human
Registry Numbers: 0
Previous Indexing: *Nuclear Proteins (2004-2020)
Heading Mapped to: *Membrane Proteins
Frequency: 37
Note: RefSeq NM_198270
Source: Am J Hum Genet 2003 Nov;73(5):1120-30
Date of Entry: 2004/08/18
Revision Date: 2019/12/19

NHS protein, human MeSH Supplementary Concept Data 2025