FOXP2 Gene

FOXP2 is a gene associated with autism and language disorders.

Lai and colleagues (2001) identified forkhead box P2 (FOXP2) as a causal gene for a severe speech and language disorder in a three-generation pedigree. Because language impairments are a hallmark of autism, the gene has been examined as a potential cause of the disorder. Results from two independent family studies, however, failed to find an association between FOXP2 and autism.

autism, gene lai, language, inheritance, foxp2, speech

  • ID: 913
  • Source: DNALC.G2C

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