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. (0000-0002-1812-7670); Ruivenkamp, C.A.L.; Alders, M.; Okamoto, N.; Bijlsma, E.K.; Plomp, A.S.; Fisher, S.E.
Published
2017
Publication type
Article / Letter to editor
FOXP1FOXP2functional characterizationneurodevelopmental disorder
Date issued
2017-11-30
Language
English
Is part of
Human Mutation (2017), Vol. 38, no. 11, p. 1542-1554
hdl
1887/116284
doi
10.1002/humu.23303