Equivalent missense variant in the FOXP2 and FOXP1 transcription factors causes distinct neurodevelopmental disorders
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Publication year
2017Source
Human Mutation, 38, 11, (2017), pp. 1542-1554ISSN
Publication type
Article / Letter to editor
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Organization
Donders Centre for Neuroscience
Neuroinformatics
Journal title
Human Mutation
Volume
vol. 38
Issue
iss. 11
Page start
p. 1542
Page end
p. 1554
Subject
NeuroinformaticsThis item appears in the following Collection(s)
- Academic publications [245054]
- Electronic publications [132354]
- Faculty of Science [37365]
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