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Q35196556-0BECF096-3F31-49CD-ACA8-132C1331D04E
Q35196556-0BECF096-3F31-49CD-ACA8-132C1331D04E
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http://www.wikidata.org/entity/statement/Q35196556-0BECF096-3F31-49CD-ACA8-132C1331D04E
Regulation of molecular pathways in the Fragile X Syndrome: insights into Autism Spectrum Disorders
P2860
Q35196556-0BECF096-3F31-49CD-ACA8-132C1331D04E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35196556-0BECF096-3F31-49CD-ACA8-132C1331D04E
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wasDerivedFrom
3d86bf4145ee0fc0ea2965cefb707ecceb7c2f2b
P2860
A deletion of 1.6 kb proximal to the CGG repeat of the FMR1 gene causes the clinical phenotype of the fragile X syndrome.