Publication
Title
Novel truncating mutations in the polyglutamine tract binding protein gene, PQBP-1, cause Renpenning syndrome and XLMR in another family with microcephaly
Author
Language
English
Source (journal)
The American journal of human genetics. - New York, N.Y.
Publication
New York, N.Y. : 2004
ISSN
0002-9297
Volume/pages
74(2004), p. 777-780
ISI
000220280800019
Full text (Publishers DOI)
Full text (open access)
UAntwerpen
Faculty/Department
Research group
Publication type
Affiliation
Publications with a UAntwerp address
External links
Web of Science
Record
Identification
Creation 08.10.2008
Last edited 02.05.2017
To cite this reference