RGD Annotation Report for fragile X syndromeRat Genome Database

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An association has been curated linking AFF2 and fragile X syndrome in Homo sapiens.

The association was inferred from experiment (EXP)
The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
16 RGD objects have been annotated to fragile X syndrome (DOID:14261)
5 papers in RGD have been used to annotate AFF2
Curation Notes: CTD Direct Evidence: marker/mechanism

RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.