A dominant variant in DMXL2 is linked to nonsyndromic hearing loss-Reference-Cited by-同舟云学术

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A dominant variant in DMXL2 is linked to nonsyndromic hearing loss

Published:2017-05 Issue:5 Volume:19 Page:553-558
ISSN:1098-3600
Container-title:Genetics in Medicine
language:en
Short-container-title:Genetics in Medicine

Author:

Chen Dong-Ye,Liu Xing-Feng,Lin Xiao-Jiang,Zhang Dan,Chai Yong-Chuan,Yu De-Hong,Sun Chang-Ling,Wang Xue-Ling,Zhu Wei-Dong,Chen Ying,Sun Lian-Hua,Wang Xiao-Wen,Shi Fu-Xin,Huang Zhi-Wu,Yang Tao,Wu Hao

Publisher

Elsevier BV

Subject

Genetics (clinical)

Link

http://www.nature.com/articles/gim2016142.pdf

Reference9 articles.

Cited by 28 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. Dmxl1 Is an Essential Mammalian Gene that Is Required for V-ATPase Assembly and Function In Vivo;Function;2024

3. Short- and long-term effects of radiation exposure at low dose and low dose rate in normal human VH10 fibroblasts;Frontiers in Public Health;2023-12-15

4. Accurate phenotypic classification and exome sequencing allow identification of novel genes and variants associated with adult-onset hearing loss;PLOS Genetics;2023-11-27

5. Rabconnectin-3α/DMXL2 Is Locally Enriched at the Synaptic Ribbon of Rod Photoreceptor Synapses;Cells;2023-06-19

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