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
Saved in:
| Main Authors: | , , |
|---|---|
| Format: | Article (Journal) |
| Language: | English |
| Published: |
2016
|
| In: |
Human molecular genetics
Year: 2015, Volume: 25, Issue: 3, Pages: 546-557 |
| ISSN: | 1460-2083 |
| DOI: | 10.1093/hmg/ddv495 |
| Online Access: | Verlag, lizenzpflichtig, Volltext: https://doi.org/10.1093/hmg/ddv495 Verlag, lizenzpflichtig, Volltext: https://academic.oup.com/hmg/article/25/3/546/2384672 
|
| Author Notes: | 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 |
| Summary: | Abstract. De novo disruptions of the neural transcription factor FOXP1 are a recently discovered, rare cause of sporadic intellectual disability (ID). We repor |
|---|---|
| Item Description: | Advance access publication date: 8 December 2015 Gesehen am 08.05.2020 |
| Physical Description: | Online Resource |
| ISSN: | 1460-2083 |
| DOI: | 10.1093/hmg/ddv495 |