Condition: Apraxia, Developmental Verbal


rs121908377 in FOXP2 gene and Apraxia, Developmental Verbal PMID 11586359 2001 A forkhead-domain gene is mutated in a severe speech and language disorder.

PMID 25232744 2014 De novo TBR1 mutations in sporadic autism disrupt protein functions.

PMID 15877281 2005 Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits.

PMID 20858596 2010 Molecular networks implicated in speech-related disorders: FOXP2 regulates the SRPX2/uPAR complex.

rs879253771 in FOXP2;MIR3666 gene and Apraxia, Developmental Verbal PMID 23918746 2013 Small intragenic deletion in FOXP2 associated with childhood apraxia of speech and dysarthria.