Analysis of the genotype–phenotype correlation of MYO15A variants in Chinese non-syndromic hearing loss patients

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Location: Deutsche Nationalbibliothek Frankfurt am Main

ISSN: 1755-8794

Extent: Online-Ressource

Language: Englisch

Notes: online resource.

Bibliographic citation: Analysis of the genotype–phenotype correlation of MYO15A variants in Chinese non-syndromic hearing loss patients ; volume:15 ; number:1 ; day:26 ; month:3 ; year:2022 ; pages:1-32 ; date:12.2022
BMC medical genomics ; 15, Heft 1 (26.3.2022), 1-32, 12.2022

Creator: Fu, Ying
Huang, Shasha
Gao, Xue
Han, Mingyu
Wang, Guojian
Kang, Dongyang
Yuan, Yongyi
Dai, Pu

Contributor: SpringerLink (Online service)

DOI: 10.1186/s12920-022-01201-3

URN: urn:nbn:de:101:1-2022061806450774432630

Rights: Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.

Last update: 15.08.2025, 7:21 AM CEST

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Fu, Ying
Huang, Shasha
Gao, Xue
Han, Mingyu
Wang, Guojian
Kang, Dongyang
Yuan, Yongyi
Dai, Pu
SpringerLink (Online service)

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Analysis of the genotype–phenotype correlation of MYO15A variants in Chinese non-syndromic hearing loss patients

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Other Objects (12)

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A biallelic variant in CLRN2 causes non-syndromic hearing loss in humans

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