A dominant variant in apoptosis-related gene XKR8 is relevant to hereditary auditory neuropathy
- Location
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Deutsche Nationalbibliothek Frankfurt am Main
- Extent
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Online-Ressource, 1 online resource.
- Language
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Englisch
- Bibliographic citation
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A dominant variant in apoptosis-related gene XKR8 is relevant to hereditary auditory neuropathy ; volume:21 ; number:1 ; day:26 ; month:4 ; year:2023 ; pages:1-8 ; date:12.2023
Journal of translational medicine ; 21, Heft 1 (26.4.2023), 1-8, 12.2023
- Creator
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Chen, Kaitian
Li, Changwu
Dong, Chang
Cen, Xiaoqing
Wang, Yueying
Liang, Yue
Zhu, Yuanping
Fang, Shubin
Jiang, Hongyan
- Contributor
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SpringerLink (Online service)
- DOI
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10.1186/s12967-023-04139-x
- URN
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urn:nbn:de:101:1-2023090410114870510062
- Rights
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
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14.08.2025, 10:59 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
- Chen, Kaitian
- Li, Changwu
- Dong, Chang
- Cen, Xiaoqing
- Wang, Yueying
- Liang, Yue
- Zhu, Yuanping
- Fang, Shubin
- Jiang, Hongyan
- SpringerLink (Online service)
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Auditory processing in individuals with auditory neuropathy
Hereditary sensory neuropathy type I
Cortical auditory evoked potentials in peripheral neuropathy
Pathogenicity of Variant m.13528A>G in MT-ND5 in Leber’s Hereditary Optic Neuropathy Is Unsupported
Autosomal dominant hereditary ataxia in Sri Lanka
Electroretinographic oscillatory potentials in Leber hereditary optic neuropathy
Screening mutations of OTOFgene in Chinese patients with auditory neuropathy, including a familial case of temperature-sensitive auditory neuropathy
Becoming familiar with hereditary transthyretin amyloidosis, a treatable neuropathy
Developments in the Treatment of Leber Hereditary Optic Neuropathy
Response to “Pathogenicity of Variant m.13528A>G in MT-ND5 in Leber’s Hereditary Optic Neuropathy Is Unsupported”
Auditory Neuropathy/Dyssynchrony: A Retrospective Analysis of 15 Cases
ATP11A causes autosomal-dominant progressive, non-syndromic auditory synaptopathy / auditory neuropathy
Auditory processing in individuals with auditory neuropathy
Hereditary sensory neuropathy type I
Cortical auditory evoked potentials in peripheral neuropathy
Pathogenicity of Variant m.13528A>G in MT-ND5 in Leber’s Hereditary Optic Neuropathy Is Unsupported
Autosomal dominant hereditary ataxia in Sri Lanka
Electroretinographic oscillatory potentials in Leber hereditary optic neuropathy
Screening mutations of OTOFgene in Chinese patients with auditory neuropathy, including a familial case of temperature-sensitive auditory neuropathy
Becoming familiar with hereditary transthyretin amyloidosis, a treatable neuropathy
Developments in the Treatment of Leber Hereditary Optic Neuropathy
Response to “Pathogenicity of Variant m.13528A>G in MT-ND5 in Leber’s Hereditary Optic Neuropathy Is Unsupported”