SnapShot: FMRP interacting proteins.
review · Level V
Where this comes from
- Record sourced from PubMed, PMID 25259928.
- Also identified by DOI 10.1016/j.cell.2014.08.036.
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Abstract
The Fragile X syndrome, caused by the absence or mutation of fragile X mental retardation protein, FMRP, is a the common component of inherited intellectual disability and autism. This SnapShot surveys the protein interaction partners of FMRP, focusing on the cellular pathways in which they are involved.
Medical subject headings
- Fragile X Messenger Ribonucleoprotein 1