Publication
Title
Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling
Author
Institution/Organisation
DDD Study
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. : 2015
ISSN
0002-9297 [print]
1537-6605 [online]
Volume/pages
97:2(2015), p. 343-352
ISI
000359328800015
Full text (Publisher's DOI)
UAntwerpen
Faculty/Department
Research group
Project info
GENCODYS: Genetic and Epigenetic Networks in Cognitive Dysfunction
Publication type
Subject
Affiliation
Publications with a UAntwerp address
External links
Web of Science
Record
Identification
Creation 05.10.2015
Last edited 19.06.2018
To cite this reference