Mutations in KCNQ4K+ channel gene, responsible for autosomal dominant hearing loss, cluster in the channel pore region.
Publication year
2000Source
American Journal of Medical Genetics, 93, 3, (2000), pp. 184-187ISSN
Publication type
Article / Letter to editor

Display more detailsDisplay less details
Organization
Otorhinolaryngology
Journal title
American Journal of Medical Genetics
Volume
vol. 93
Issue
iss. 3
Page start
p. 184
Page end
p. 187
Subject
Genetics of hearing; Erfelijk gehoorverliesThis item appears in the following Collection(s)
- Academic publications [227425]
- Faculty of Medical Sciences [86157]
Upload full text
Use your RU credentials (u/z-number and password) to log in with SURFconext to upload a file for processing by the repository team.