Publication
Title
Mutations in the Wolfram syndrome 1 gene (WFS1) are a common cause of low frequency sensorineural hearing loss
Author
Language
English
Source (journal)
Human molecular genetics. - Oxford
Publication
Oxford : 2001
ISSN
0964-6906
Volume/pages
10:22(2001), p. 2501-2508
ISI
000172446300004
Full text (Publisher's DOI)
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 01.10.2017
To cite this reference