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  1. Article

    Open Access

    FOXP1 syndrome: a review of the literature and practice parameters for medical assessment and monitoring

    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 m...

    Reymundo Lozano, Catherine Gbekie… in Journal of Neurodevelopmental Disorders (2021)

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