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- Search Terms:ISSN: 10976256AndISSN: 15461726AndVolume Number: 14AndIssue Number: 12AndStart Page: 1517AndDate: 2011 Revise Search
- 1From: Nature Neuroscience. (Vol. 14, Issue 12) Peer-ReviewedLoss of FMR1 gene function results in fragile X syndrome, the most common heritable form of intellectual disability. The protein encoded by this locus (FMRP) is an RNA-binding protein that is thought to primarily act as...