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 / American Society of Human Genetics [Bethesda, Md] - New York, N.Y., 1949, currens
Publication
New York, N.Y. : 2004
ISSN
0002-9297 [print]
1537-6605 [online]
DOI
10.1086/383205
Volume/pages
74 (2004) , p. 777-780
ISI
000220280800019
Full text (Publisher's DOI)
Full text (open access)
UAntwerpen
Faculty/Department
Research group
Project info
Publication type
Affiliation
Publications with a UAntwerp address
External links
Web of Science
Record
Identifier
Creation 08.10.2008
Last edited 23.08.2022
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