Four novelTMC1 (DFNB7/DFNB11) mutations in Turkish patients with congenital autosomal recessive nonsyndromic hearing loss-Reference-Cited by-同舟云学术

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Four novelTMC1 (DFNB7/DFNB11) mutations in Turkish patients with congenital autosomal recessive nonsyndromic hearing loss

Published:2005 Issue:6 Volume:26 Page:591-591
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Kalay E.,Karaguzel A.,Caylan R.,Heister A.,Cremers F.P.M.,Cremers C.W.R.J.,Brunner H.G.,de Brouwer A.P.M.,Kremer H.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Cited by 47 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. Functional consequences of Genetics variant in TMC1 and TMC2 within a United Arab Emirates family with Pre-lingual hearing loss;Saudi Journal of Biological Sciences;2023-02

2. A Short Overview on Hearing Loss and Related Auditory Defects;Auditory System - Function and Disorders;2022-09-28

3. An update on autosomal recessive hearing loss and loci involved in it;Indian Journal of Otology;2022

4. Prevalence and clinical features of autosomal dominant and recessive TMC1-associated hearing loss;Human Genetics;2021-09-14

5. Novel homozygous variants in the TMC1 and CDH23 genes cause autosomal recessive nonsyndromic hearing loss;Molecular Genetics & Genomic Medicine;2020-11-18

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