MeSH Browser

MeSH Supplementary: FXR1 protein, human
Unique ID: C096916
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C096916
Entry Term(s): fragile X mental retardation syndrome related protein 1, human; fragile X mental retardation, autosomal homolog 1, human
Registry Numbers: 0
Heading Mapped to: *RNA-Binding Proteins
Frequency: 139
Note: RefSeq NM_005087
Source: EMBO J 1995 Nov 1;14(21):5358-66
Indexing Information: Fragile X Syndrome; Fragile X Mental Retardation Protein
Date of Entry: 1995/12/28
Revision Date: 2006/05/22

FXR1 protein, human MeSH Supplementary Concept Data 2025