Title
A splice-site mutation and overexpression of **MYO6** cause a similar phenotype in two families with autosomal dominant hearing loss A splice-site mutation and overexpression of **MYO6** cause a similar phenotype in two families with autosomal dominant hearing loss
Author
Faculty/Department
Faculty of Medicine and Health Sciences
Faculty of Pharmaceutical, Biomedical and Veterinary Sciences . Biomedical Sciences
Publication type
article
Publication
Leiden ,
Source (journal)
European journal of human genetics / European Society of Human Genetics. - Leiden
Volume/pages
16(2008) :5 , p. 593-602
ISSN
1018-4813
ISI
000255260500010
General
doi: 10.1038/sj.ejhg.5202000
Carrier
E
Target language
English (eng)
Full text (Publishers DOI)
Affiliation
University of Antwerp
E-info
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Handle