A novel MYO6 splice site mutation causes autosomal dominant sensorineural hearing loss type DFNA22 with a favourable outcome after cochlear implantation
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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Online-Ressource
- Language
-
Englisch
- Bibliographic citation
-
In: Audiology and Neurotology ; 18 (2013), 3. - S. 192-199. - ISSN 1420-3030. - eISSN 1421-9700
- Keyword
-
Hörverlust
Cochlear-Implantat
Molekularer Motor
Myosin
- Event
-
Veröffentlichung
- (where)
-
Ulm
- (who)
-
Universität Ulm
- (when)
-
2013
- Creator
-
Volk, Alexander E.
Lang-Roth, Ruth
Yigit, Goekhan
Borck, Guntram
Nuernberg, Gudrun
Rosenkranz, Stephan
Nuernberg, Peter
Kubisch, Christian
Beutner, Dirk
- DOI
-
10.18725/OPARU-40441
- URN
-
urn:nbn:de:bsz:289-oparu-40517-4
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
15.08.2025, 7:30 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Volk, Alexander E.
- Lang-Roth, Ruth
- Yigit, Goekhan
- Borck, Guntram
- Nuernberg, Gudrun
- Rosenkranz, Stephan
- Nuernberg, Peter
- Kubisch, Christian
- Beutner, Dirk
- Universität Ulm
Time of origin
- 2013
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MPZL2—a common autosomal recessive deafness gene related to moderate sensorineural hearing loss in the Chinese population
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