High prevalence of CDH23 mutations in patients with congenital high-frequency sporadic or recessively inherited hearing loss
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
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1750-1172
- Extent
-
Online-Ressource
- Language
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Englisch
- Notes
-
online resource.
- Bibliographic citation
-
High prevalence of CDH23 mutations in patients with congenital high-frequency sporadic or recessively inherited hearing loss ; volume:10 ; number:1 ; day:13 ; month:5 ; year:2015 ; pages:1-9 ; date:12.2015
Orphanet journal of rare diseases ; 10, Heft 1 (13.5.2015), 1-9, 12.2015
- Creator
-
Mizutari, Kunio
Mutai, Hideki
Namba, Kazunori
Miyanaga, Yuko
Nakano, Atsuko
Arimoto, Yukiko
Masuda, Sawako
Morimoto, Noriko
Sakamoto, Hirokazu
Kaga, Kimitaka
Matsunaga, Tatsuo
- Contributor
-
SpringerLink (Online service)
- DOI
-
10.1186/s13023-015-0276-z
- URN
-
urn:nbn:de:101:1-2021081922052366219908
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:48 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
- Mizutari, Kunio
- Mutai, Hideki
- Namba, Kazunori
- Miyanaga, Yuko
- Nakano, Atsuko
- Arimoto, Yukiko
- Masuda, Sawako
- Morimoto, Noriko
- Sakamoto, Hirokazu
- Kaga, Kimitaka
- Matsunaga, Tatsuo
- SpringerLink (Online service)
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