Novel compound heterozygous mutations in the OTOF Gene identified by whole-exome sequencing in auditory neuropathy spectrum disorder

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1471-2350

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Novel compound heterozygous mutations in the OTOF Gene identified by whole-exome sequencing in auditory neuropathy spectrum disorder ; volume:18 ; number:1 ; day:23 ; month:3 ; year:2017 ; pages:1-7 ; date:12.2017
BMC medical genetics ; 18, Heft 1 (23.3.2017), 1-7, 12.2017

Keyword: Gehörlosigkeit
Ohrenkrankheit
Audiologie
Ohrenheilkunde

Creator: Tang, Fengzhu

Contributor: Ma, DengKe
Wang, Yulan
Qiu, Yuecai
Liu, Fei
Wang, Qingqing
Lu, Qiutian
Shi, Min
Xu, Liang
Liu, Min
Liang, Jianping
SpringerLink (Online service)

DOI: 10.1186/s12881-017-0400-0

URN: urn:nbn:de:1111-20170413975

Rights: Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 14.08.2025, 10:55 AM CEST

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Tang, Fengzhu
Ma, DengKe
Wang, Yulan
Qiu, Yuecai
Liu, Fei
Wang, Qingqing
Lu, Qiutian
Shi, Min
Xu, Liang
Liu, Min
Liang, Jianping
SpringerLink (Online service)

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Novel compound heterozygous mutations in the OTOF Gene identified by whole-exome sequencing in auditory neuropathy spectrum disorder

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