Radboud Repository
Radboud Repository
→
Collections Radboud University
→
Academic publications
→
View Item
JavaScript is disabled for your browser. Some features of this site may not work without it.
There is no fulltext present in this item.
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
Display more details
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
This item appears in the following Collection(s)
Faculty of Science
[28757]
Academic publications
[186034]
Academic output Radboud University
Search Repository
Search Repository
This Collection
Browse
All of Repository
Collections
Departments
Date Issued
Authors
Titles
Document type
This Collection
Departments
Date Issued
Authors
Titles
Document type
Statistics
View Item Statistics