Identification of OSBPL2 as a novel candidate gene for progressive nonsyndromic hearing loss by whole-exome sequencing-Reference-Cited by-同舟云学术

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Identification of OSBPL2 as a novel candidate gene for progressive nonsyndromic hearing loss by whole-exome sequencing

Published:2015-03 Issue:3 Volume:17 Page:210-218
ISSN:1098-3600
Container-title:Genetics in Medicine
language:en
Short-container-title:Genetics in Medicine

Author:

Xing Guangqian,Yao Jun,Wu Bin,Liu Tingting,Wei Qinjun,Liu Cheng,Lu Yajie,Chen Zhibin,Zheng Heng,Yang Xiaonan,Cao Xin

Publisher

Elsevier BV

Subject

Genetics (clinical)

Link

http://www.nature.com/articles/gim201490.pdf

Reference40 articles.

1. Hereditary hearing loss and its syndromes.;Cohen,1995

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3. Impact of cholesterol homeostasis within cochlear cells on auditory development and hearing loss;Frontiers in Cellular Neuroscience;2024-01-04

4. The applications of CRISPR/Cas-mediated genome editing in genetic hearing loss;Cell & Bioscience;2023-05-20

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