In-depth characterisation of a cohort of individuals with missense and loss-of-function variants disruptingFOXP2

Overview of attention for article published in Journal of Medical Genetics, November 2022

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Indepth characterization of a cohort of individuals with missense and loss-of-function variants disrupting FOXP2

JMG Contact blog, 04 Nov 2022

Heterozygous disruptions of FOXP2 were the first identified molecular cause for severe speech disorder; childhood apraxia of…

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