MeSH Browser

MeSH Supplementary: AMMECR1 protein, human
Unique ID: C118927
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C118927
Entry Term(s): Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region, gene 1 protein, human
Registry Numbers: 0
Heading Mapped to: *Proteins
Frequency: 9
Note: RefSeq NM_001025580
Source: Genomics 1999 Feb 1;55(3):335-40
Date of Entry: 1999/05/21
Revision Date: 2006/05/05

AMMECR1 protein, human MeSH Supplementary Concept Data 2025