Equivalent missense variant in the FOXP2 and FOXP1 transcription factors causes distinct neurodevelopmental disorders

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Title:	Equivalent missense variant in the FOXP2 and FOXP1 transcription factors causes distinct neurodevelopmental disorders
Author(s):	Sollis, E.; Deriziotis, P.; Saitsu, H.; Miyake, N.; Matsumoto, N.; Hoffer, M.J.V.; Ruivenkamp, C.A.L.; Alders, M.; Okamoto, N.; Bijlsma, E.K.; Plomp, A.S.; Fisher, S.E.
Publication year:	2017
Source:	Human Mutation, vol. 38, iss. 11, (2017), pp. 1542-1554
ISSN:	1059-7794
DOI:	https://doi.org/10.1002/humu.23303
Publication type:	Article / Letter to editor
Please use this identifier to cite or link to this item : https://hdl.handle.net/2066/178956
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Subject:	Neuroinformatics
Organization:	Donders Centre for Neuroscience Neuroinformatics
Journal title:	Human Mutation
Volume:	vol. 38
Issue:	iss. 11
Page start:	p. 1542
Page end:	p. 1554