Identification and functional characterization of de novo FOXP1 variants provides novel insights into the etiology of neurodevelopmental disorder
Abstract. De novo disruptions of the neural transcription factor FOXP1 are a recently discovered, rare cause of sporadic intellectual disability (ID). We repor
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| Hauptverfasser: | , , |
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| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
2016
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| In: |
Human molecular genetics
Year: 2015, Jahrgang: 25, Heft: 3, Pages: 546-557 |
| ISSN: | 1460-2083 |
| DOI: | 10.1093/hmg/ddv495 |
| Online-Zugang: | Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1093/hmg/ddv495 Verlag, lizenzpflichtig, Volltext: https://academic.oup.com/hmg/article/25/3/546/2384672 
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| Verfasserangaben: | 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 and Simon E. Fisher |
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| 520 | |a Abstract. De novo disruptions of the neural transcription factor FOXP1 are a recently discovered, rare cause of sporadic intellectual disability (ID). We repor | ||
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