A novel frameshift mutation of POU4F3 gene associated with autosomal dominant non-syndromic hearing loss-Reference-Cited by-同舟云学术

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A novel frameshift mutation of POU4F3 gene associated with autosomal dominant non-syndromic hearing loss

Published:2010-06 Issue:3 Volume:396 Page:626-630
ISSN:0006-291X
Container-title:Biochemical and Biophysical Research Communications
language:en
Short-container-title:Biochemical and Biophysical Research Communications

Author:

Lee Hee Keun,Park Hong-Joon,Lee Kyu-Yup,Park Rekil,Kim Un-Kyung

Funder

Ministry of Education, Science and Technology

Ministry of Education, Science & Technology (MEST)/National Research Foundation of Korea (NRF)

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

Reference22 articles.

1. Genetic epidemiology of hearing impairment;Morton;Ann. NY Acad. Sci.,1991

2. A novel locus DFNA59 for autosomal dominant nonsyndromic hearing loss maps at chromosome 11p14.2-q12.3;Chatterjee;Hum. Genet.,2009

3. From deafness genes to hearing mechanisms: harmony and counterpoint;Petit;Trends Mol. Med.,2006

4. Mutation in transcription factor POU4F3 associated with inherited progressive hearing loss in humans;Vahava;Science,1998

5. Role of transcription factors Brn-3.1 and Brn-3.2 in auditory and visual system development;Erkman;Nature,1996

Cited by 28 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Autosomal Dominant Non-Syndromic Hearing Loss (DFNA): A Comprehensive Narrative Review;Biomedicines;2023-06-01

2. Highly variable hearing loss due to POU4F3 (c.37del) is revealed by longitudinal, frequency specific analyses;European Journal of Human Genetics;2023-04-19

3. A Missense POU4F3 Variant Associated with Autosomal Dominant Midfrequency Hearing Loss Alters Subnuclear Localization and Transcriptional Capabilities;BioMed Research International;2021-06-21

4. Cochlear implantation in a patient with a POU4F3 mutation;Clinical Case Reports;2020-11-11

5. Aldh inhibitor restores auditory function in a mouse model of human deafness;PLOS Genetics;2020-09-24

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