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

Elliot Sollis, Sarah A. Graham, Arianna Vino, Henning Froehlich, Maaike Vreeburg, Danai Dimitropoulou, Christian Gilissen, Rolph Pfundt, Gudrun A. Rappold, Han G. Brunner, Pelagia Deriziotis, Simon E. Fisher

Research output: Contribution to journalArticleAcademicpeer-review

Original languageEnglish
Pages (from-to)546-557
JournalHuman Molecular Genetics
Issue number3
Publication statusPublished - 1 Feb 2016

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