Novel compound heterozygous mutations in the MYO15A gene in autosomal recessive hearing loss identified by whole-exome sequencing

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1479-5876

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Novel compound heterozygous mutations in the MYO15A gene in autosomal recessive hearing loss identified by whole-exome sequencing ; volume:11 ; number:1 ; day:9 ; month:11 ; year:2013 ; pages:1-7 ; date:12.2013
Journal of translational medicine ; 11, Heft 1 (9.11.2013), 1-7, 12.2013

Creator: Gao, Xue

Contributor: Zhu, Qing-yan
Song, Yue-Shuai
Wang, Guo-Jian
Yuan, Yong-yi
Xin, Feng
Huang, Sha-sha
Kang, Dong-Yang
Han, Ming-Yu
Guan, Li-ping
Zhang, Jian-Guo
Dai, Pu
SpringerLink (Online service)

DOI: 10.1186/1479-5876-11-284

URN: urn:nbn:de:1111-2016041444866

Rights: Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 14.08.2025, 10:53 AM CEST

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Associated

Gao, Xue
Zhu, Qing-yan
Song, Yue-Shuai
Wang, Guo-Jian
Yuan, Yong-yi
Xin, Feng
Huang, Sha-sha
Kang, Dong-Yang
Han, Ming-Yu
Guan, Li-ping
Zhang, Jian-Guo
Dai, Pu
SpringerLink (Online service)

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Novel compound heterozygous mutations in the MYO15A gene in autosomal recessive hearing loss identified by whole-exome sequencing

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Other Objects (12)

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Novel compound heterozygous MYO15A splicing variants in autosomal recessive non-syndromic hearing loss

Autosomal recessive cerebellar ataxias

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