Publication
Title
A splice-site mutation and overexpression of **MYO6** cause a similar phenotype in two families with autosomal dominant hearing loss
Author
Language
English
Source (journal)
European journal of human genetics / European Society of Human Genetics. - Leiden
Publication
Leiden : 2008
ISSN
1018-4813
Volume/pages
16:5(2008), p. 593-602
ISI
000255260500010
Note
General: doi: 10.1038/sj.ejhg.5202000
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 19.11.2017
To cite this reference