Novel sequence variants in theTMC1 gene in Pakistani families with autosomal recessive hearing impairment-Reference-Cited by-同舟云学术

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Novel sequence variants in theTMC1 gene in Pakistani families with autosomal recessive hearing impairment

Published:2005 Issue:4 Volume:26 Page:396-396
ISSN:1059-7794
Container-title:Human Mutation
language:en
Short-container-title:Hum. Mutat.

Author:

Santos Regie Lyn P.,Wajid Muhammad,Khan Mohammad Nasim,McArthur Nathan,Pham Thanh L.,Bhatti Attya,Lee Kwanghyuk,Irshad Saba,Mir Asif,Yan Kai,Chahrour Maria H.,Ansar Muhammad,Ahmad Wasim,Leal Suzanne M.

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Cited by 52 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. Clinical Genetic Testing for Hearing Loss: Implications for Genetic Counseling and Gene-Based Therapies;Biomedicines;2024-06-27

2. Biallelic mutations in pakistani families with autosomal recessive prelingual nonsyndromic hearing loss;Genes & Genomics;2022-12-06

3. A novel splicing variant in the TMC1 gene causes non-syndromic hearing loss in a Chinese family;Chinese Medical Journal;2022-01-27

4. Identification of homozygous mutations for hearing loss;Gene;2021-04

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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