Mutations in ACTL6B Cause Neurodevelopmental Deficits and Epilepsy and Lead to Loss of Dendrites in Human Neurons

Fulltext:
203584.pdf
Embargo:
until further notice
Size:
4.629Mb
Format:
PDF
Description:
Publisher’s version
Publication year
2019Source
American Journal of Human Genetics, 104, 5, (2019), pp. 815-834ISSN
Publication type
Article / Letter to editor

Display more detailsDisplay less details
Organization
Human Genetics
Journal title
American Journal of Human Genetics
Volume
vol. 104
Issue
iss. 5
Page start
p. 815
Page end
p. 834
Subject
All institutes and research themes of the Radboud University Medical Center; Radboudumc 7: Neurodevelopmental disorders DCMN: Donders Center for Medical NeuroscienceThis item appears in the following Collection(s)
- Academic publications [227425]
- Electronic publications [107155]
- Faculty of Medical Sciences [86157]
Upload full text
Use your RU credentials (u/z-number and password) to log in with SURFconext to upload a file for processing by the repository team.