Identification of four TMC1 variations in different Chinese families with hereditary hearing loss-Reference-Cited by-同舟云学术

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Identification of four TMC1 variations in different Chinese families with hereditary hearing loss

Published:2018-04-14 Issue:4 Volume:6 Page:504-513
ISSN:2324-9269
Container-title:Molecular Genetics & Genomic Medicine
language:en
Short-container-title:Mol Genet Genomic Med

Author:

Wang Hongyang¹,Wu Kaiwen¹,Guan Jing¹,Yang Ju¹,Xie Linyi¹,Xiong Fen¹,Lan Lan¹,Wang Dayong¹,Wang Qiuju¹^ORCID

Affiliation:

1. Institute of Otolaryngology; Chinese PLA General Hospital; Medical School of Chinese PLA; Beijing China

Funder

National Natural Science Foundation of China

National Key Basic Research Program of China

China Postdoctoral Science Foundation

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/mgg3.394/fullpdf

Reference42 articles.

1. Tmc gene therapy restores auditory function in deaf mice;Askew;Science Translational Medicine,2015

2. Comprehensive analysis via exome sequencing uncovers genetic etiology in autosomal recessive nonsyndromic deafness in a large multiethnic cohort;Bademci;Genetics in Medicine,2016

3. A novel mutation in the TMC1 gene causes non-syndromic hearing loss in a Moroccan family;Bakhchane;Gene,2015

4. Targeted genomic capture and massively parallel sequencing to identify genes for hereditary hearing loss in Middle Eastern families;Brownstein;Genome Biology,2011

5. tmc-1 encodes a sodium-sensitive channel required for salt chemosensation in C. elegans;Chatzigeorgiou;Nature,2013

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1. CIB2 as a Ca²⁺Sensor for Auditory Mechano-Electrical Transduction and Linked to Genetic-Heterogeneity ofTMC1in Hearing Loss;2024-07-24

2. Clinical and genetic architecture of a large cohort with auditory neuropathy;Human Genetics;2024-03

3. Genetic correction of induced pluripotent stem cells from a DFNA36 patient results in morphologic and functional recovery of derived hair cell-like cells;Stem Cell Research & Therapy;2024-01-02

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

5. Generation of a gene corrected human isogenic iPSC line (CPGHi001-A-1) from a hearing loss patient with the TMC1 p.M418K mutation using CRISPR/Cas9;Stem Cell Research;2022-04

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