MeSH Browser

MeSH Supplementary: FMR3 protein, human
Unique ID: C419105
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C419105
Entry Term(s): fragile X mental retardation associated 3 protein, human
Registry Numbers: 0
Heading Mapped to: *Proteins
Frequency: 2
Note: associated with FRAXE mental retardation; amino acid sequence in first source
Source: J Med Genet 2000 Oct;37(10):782-4
Indexing Information: Fragile X Mental Retardation Protein
Date of Entry: 2001/01/30
Revision Date: 2005/07/29

FMR3 protein, human MeSH Supplementary Concept Data 2025