Source: BEFREE

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 93986
Gene Symbol: FOXP2
FOXP2
CUI: C1845668
Disease: Perisylvian syndrome
Perisylvian syndrome 		0.010 GeneticVariation BEFREE Mutations in transcription factor FOXP2 cause difficulties mastering fluent speech (developmental verbal dyspraxia, DVD), whereas mutations of sushi-repeat protein SRPX2 lead to epilepsy of the rolandic (sylvian) speech areas, with DVD or with bilateral perisylvian polymicrogyria. 20858596

2010