WebApr 23, 2024 · FOXP1 syndrome is a neurodevelopmental disorder caused by mutations or deletions that disrupt the forkhead box protein 1 ( FOXP1) gene, which encodes a transcription factor important for the early development of many organ systems, including the … WebJul 1, 2013 · Aberrant language development is one of the clinical characteristics of autism. Mutations of FOXP2 have been linked to speech and language disorders and ASD [36–38].FOXP1 is a member of subfamily P of the forkhead box (FOX) transcription factor family and forms a heterodimer with FOXP2 [39, 40].The elevated mRNA level of FOXP1 …
Autism spectrum disorder - Symptoms and causes - Mayo Clinic
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Autism Spectrum Disorder Service NYU Langone Health
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