Novel Molecular Genetic Etiology of Asymmetric Hearing Loss: Autosomal-Dominant LMX1A Variants-Reference-Cited by-同舟云学术

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Novel Molecular Genetic Etiology of Asymmetric Hearing Loss: Autosomal-Dominant LMX1A Variants

Published:2022-06-17 Issue:6 Volume:43 Page:1698-1707
ISSN:1538-4667
Container-title:Ear & Hearing
language:en
Short-container-title:

Author:

Lee Sang-Yeon,Soon Yoo Hyo,Hee Han Jin,Hee Lee Dae,Soo Park Sang,Hwan Suh Myung,Ho Lee Jun,Oh Seung-Ha,Choi Byung Yoon

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Speech and Hearing,Otorhinolaryngology

Reference35 articles.

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2. Unilateral cochlear nerve deficiency in children.;Clemmens;Otolaryngol Head Neck Surg,2013

3. Tbx6 controls left-right asymmetry through regulation of Gdf1.;Concepcion;Biol Open,2018

4. Inner ear gene therapies take off: Current promises and future challenges.;Delmaghani;J Clin Med,2020

5. TEADs, Yap, Taz, Vgll4s transcription factors control the establishment of Left-Right asymmetry in zebrafish.;Fillatre;Elife,2019

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1. Functional pathogenicity of ESRRB variant of uncertain significance contributes to hearing loss (DFNB35);Scientific Reports;2024-09-11

2. Updates on Genetic Hearing Loss: From Diagnosis to Targeted Therapies;Journal of Audiology and Otology;2024-04-10

3. Novel autosomal dominant TMC1 variants linked to hearing loss: insight into protein-lipid interactions;BMC Medical Genomics;2023-12-08

4. Allelic hierarchy for USH2A influences auditory and visual phenotypes in South Korean patients;Scientific Reports;2023-11-19

5. Phenotypic and molecular basis of SIX1 variants linked to non-syndromic deafness and atypical branchio-otic syndrome in South Korea;Scientific Reports;2023-07-21

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