Functional consequences of Genetics variant in TMC1 and TMC2 within a United Arab Emirates family with Pre-lingual hearing loss

Author:

Al Mutery Abdullah,Kamal Eldin Mohamed Walaa,Mahfood Mona,Chouchen Jihen,Tlili Abdelaziz

Funder

University of Sharjah

Publisher

Elsevier BV

Subject

General Agricultural and Biological Sciences

Reference31 articles.

1. A Novel Mutation in the TMC1 Gene Causes Nonsyndromic Hearing Loss in a Moroccan Family;Bakhchane;Gene,2015

2. Structural relationship between the putative hair cell mechanotransduction channel TMC1 and TMEM16 proteins;Ballesteros;Elife,2018

3. Whole-Exome Sequencing Efficiently Detects Rare Mutations in Autosomal Recessive Nonsyndromic Hearing Loss;Diaz-Horta;PLoS One,2012

4. CIB2 interacts with TMC1 and TMC2 and is essential for mechanotransduction in auditory hair cells;Giese;Nature communications,2017

5. Global Costs of Unaddressed Hearing Loss and Cost-Effectiveness of Interven- tions Available online: https://www.who.int/publications-detail-redirect/global-costs-of-unaddressed-hearing-loss-and-cost-effectiveness-of-interventions (accessed on 15 September 2021).

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