MeSH Browser

MeSH Supplementary: MRPS22 protein, human
Unique ID: C526186
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C526186
Registry Numbers: 0
Heading Mapped to: *Ribosomal Proteins; *Mitochondrial Proteins
Frequency: 10
Note: mutation in this protein causes antenatal mitochondrial disease; GenBank AF226045
Source: J Med Genet 2007 Dec;44(12):784-6
Date of Entry: 2008/01/31
Revision Date: 1955/01/01

MRPS22 protein, human MeSH Supplementary Concept Data 2025