Nonsense mutation of the stereociliar membrane protein gene PTPRQ in human hearing loss DFNB84-Reference-Cited by-同舟云学术

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Nonsense mutation of the stereociliar membrane protein gene PTPRQ in human hearing loss DFNB84

Published:2010-05-14 Issue:9 Volume:47 Page:643-645
ISSN:0022-2593
Container-title:Journal of Medical Genetics
language:en
Short-container-title:Journal of Medical Genetics

Author:

Shahin H.,Rahil M.,Rayan A. A.,Avraham K. B.,King M.-C.,Kanaan M.,Walsh T.

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Cited by 39 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. Novel PTPRQ variants associated with hearing loss in a Chinese family PTPRQ variants in Chinese hearing loss;Frontiers in Genetics;2024-08-14

2. Detailed Clinical Features of PTPRQ-Associated Hearing Loss Identified in a Large Japanese Hearing Loss Cohort;Genes;2024-04-12

3. Cerebrospinal fluid biomarkers for normal pressure hydrocephalus;Biomarkers in Neuropsychiatry;2023-12

4. Delayed progressive sensorineural hearing loss due to a novel compound heterozygous PTPRQ mutation in a Chinese patient;Journal of Clinical Laboratory Analysis;2023-04

5. Hereditable variants of classical protein tyrosine phosphatase genes: Will they prove innocent or guilty?;Frontiers in Cell and Developmental Biology;2023-01-23

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