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
DOI
10.1093/HMG/10.22.2501
Volume/pages
10 :22 (2001) , p. 2501-2508
ISI
000172446300004
Full text (Publisher's DOI)
UAntwerpen
Faculty/Department
Publication type
Affiliation
Publications with a UAntwerp address
External links
Web of Science
Record
Identifier
Creation 08.10.2008
Last edited 04.03.2024
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