A novel early truncation mutation in OTOG causes prelingual mild hearing loss without vestibular dysfunction-Reference-Cited by-同舟云学术

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A novel early truncation mutation in OTOG causes prelingual mild hearing loss without vestibular dysfunction

Published:2019-01 Issue:1 Volume:62 Page:81-84
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Yu Seyoung,Choi Hye Ji,Lee Joon Suk,Lee Hyun Jae,Rim John Hoon,Choi Jae Young,Gee Heon Yung^ORCID,Jung Jinsei

Funder

Basic Science Research Program

National Research Foundation of Korea

Ministry of Education

Korea government

Ministry of Health & Welfare, Republic of Korea

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics,General Medicine

Reference11 articles.

1. Vestibular function is associated with residual low-frequency hearing loss in patients with bi-allelic mutations in the SLC26A4 gene;Jung;Hear. Res.,2016

2. Genetic predisposition to sporadic congenital hearing loss in a pediatric population;Jung;Sci. Rep.,2017

3. Hereditary hearing loss: from human mutation to mechanism;Lenz;Hear. Res.,2011

4. Mutations in COL11A2 cause non-syndromic hearing loss (DFNA13);McGuirt;Nat. Genet.,1999

5. Newborn hearing screening–a silent revolution;Morton;N. Engl. J. Med.,2006

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1. Identification of novel likely pathogenic variant in CDH23 causing non-syndromic hearing loss, and a novel variant in OTOGL in an extended Iranian family;Egyptian Journal of Medical Human Genetics;2024-09-14

2. The cochlear matrisome: Importance in hearing and deafness;Matrix Biology;2024-01

3. Identification and computational analysis of USH1C, and SLC26A4 variants in Pakistani families with prelingual hearing loss;Molecular Biology Reports;2020-11-24

4. Burden of Rare Variants in the OTOG Gene in Familial Meniere’s Disease;Ear & Hearing;2020-04-02

5. Compound Phenotype Due to Recessive Variants in LARP7 and OTOG Genes Disclosed by an Integrated Approach of SNP-Array and Whole Exome Sequencing;Genes;2020-03-31

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