De novo and bi-allelic variants in AP1G1 cause neurodevelopmental disorder with developmental delay, intellectual disability, and epilepsy

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Publication year
2021Source
American Journal of Human Genetics, 108, 7, (2021), pp. 1330-1341ISSN
Publication type
Article / Letter to editor

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Organization
Human Genetics
Cognitive Neuroscience
Journal title
American Journal of Human Genetics
Volume
vol. 108
Issue
iss. 7
Page start
p. 1330
Page end
p. 1341
Subject
Radboudumc 7: Neurodevelopmental disorders DCMN: Donders Center for Medical NeuroscienceThis item appears in the following Collection(s)
- Academic publications [227437]
- Electronic publications [107154]
- Faculty of Medical Sciences [86157]
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