Title : Absence of causative mutations and presence of autism-related allele in FOXP2 in Japanese autistic patients.

Pub. Date : 2005 Apr

PMID : 15737702






1 Functional Relationships(s)
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1 We analyzed the FOXP2 gene, which encodes a putative transcription factor containing a polyglutamine tract and a forkhead DNA-binding domain, for a possible causative mutation in autism. polyglutamine forkhead box P2 Homo sapiens