Publication
Title
De novo loss-of-function mutations in CHD2 cause a fever-sensitive myoclonic epileptic encephalopathy sharing features with Dravet syndrome
Author
Institution/Organisation
EuroEPINOMICS RES Consortium
Abstract
Language
English
Source (journal)
The American journal of human genetics / American Society of Human Genetics [Bethesda, Md] - New York, N.Y., 1949, currens
Publication
New York, N.Y. : 2013
ISSN
0002-9297 [print]
1537-6605 [online]
Volume/pages
93:5(2013), p. 967-975
ISI
000326996600017
Full text (Publisher's DOI)
UAntwerpen
Faculty/Department
Research group
Publication type
Subject
Affiliation
Publications with a UAntwerp address
External links
Web of Science
Record
Identification
Creation 15.01.2014
Last edited 29.08.2018
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