A novel missense mutation in SMPX causes a rare form of X-linked postlingual sensorineural hearing loss in a Chinese family-Reference-Cited by-同舟云学术

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A novel missense mutation in SMPX causes a rare form of X-linked postlingual sensorineural hearing loss in a Chinese family

Published:2021-02 Issue:2 Volume:10 Page:378-387
ISSN:2224-4336
Container-title:Translational Pediatrics
language:
Short-container-title:Transl Pediatr

Author:

Guo Yingyuan,Hao Yanru,Zhang Dejun,Xu Hongen,Yu Duojiao,Lv Jingmao,Fu Zeming,Han Shuang,Guo Fang,Bai Jie,Guan Guofang

Publisher

AME Publishing Company

Subject

Pediatrics, Perinatology and Child Health

Link

https://tp.amegroups.com/article/download/61858/pdf

Cited by 3 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. Differentiation and functioning of the lateral line organ in zebrafish require Smpx activity;Scientific Reports;2024-04-03

2. Inner Ear and Muscle Developmental Defects in Smpx-Deficient Zebrafish Embryos;International Journal of Molecular Sciences;2021-06-17

3. Missense mutations in small muscle protein X-linked (SMPX) cause distal myopathy with protein inclusions;Acta Neuropathologica;2021-05-11

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