MeSH Browser

MeSH Supplementary: Ammecr1 protein, mouse
Unique ID: C485590
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C485590
Entry Term(s): Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1 homolog (human) protein, mouse
Registry Numbers: 0
Heading Mapped to: *Proteins
Frequency: 2
Note: RefSeq NM_019496
Date of Entry: 2004/08/06
Revision Date: 2011/07/15

Ammecr1 protein, mouse MeSH Supplementary Concept Data 2025