Identification and functional characterization of de novo FOXP1 variants provides novel insights into the etiology of neurodevelopmental disorder (Q28115816)

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Identification and functional characterization of de novo FOXP1 variants provides novel insights into the etiology of neurodevelopmental disorder
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    Identification and functional characterization of de novo FOXP1 variants provides novel insights into the etiology of neurodevelopmental disorder (English)

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