A novel NHS mutation in a Chinese family with Nance‑Horan Syndrome-Reference-Cited by-同舟云学术

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A novel NHS mutation in a Chinese family with Nance‑Horan Syndrome

Published:2019-03-29 Issue: Volume: Page:
ISSN:1791-2997
Container-title:Molecular Medicine Reports
language:
Short-container-title:Mol Med Report

Author:

Wei Meirong¹,Qi Anhui²,Mo Haiming¹,Wu Kailin¹,Ma Xu³,Wang Binbin²

Affiliation:

1. Department of Ophthalmology, Liuzhou Maternal and Child Healthcare Hospital, Liuzhou, Guangxi 545001, P.R. China

2. Graduate School of Peking Union Medical College, Beijing 100730, P.R. China

3. Center for Genetics, National Research Institute for Family Planning, Beijing 100081, P.R. China

Publisher

Spandidos Publications

Subject

Cancer Research,Oncology,Genetics,Molecular Biology,Molecular Medicine,Biochemistry

Cited by 2 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. Genetic research on Nance-Horan syndrome caused by a novel mutation in the NHS gene;Gene;2024-05

2. A novel Nance-Horan syndrome mutation identified by next-generation sequencing in a Chinese family;International Journal of Ophthalmology;2022-06-18

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