Mutations of P4HA2 encoding prolyl 4-hydroxylase 2 are associated with nonsyndromic high myopia-Reference-Cited by-同舟云学术

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Mutations of P4HA2 encoding prolyl 4-hydroxylase 2 are associated with nonsyndromic high myopia

Published:2015-04 Issue:4 Volume:17 Page:300-306
ISSN:1098-3600
Container-title:Genetics in Medicine
language:en
Short-container-title:Genetics in Medicine

Author:

Guo Hui,Tong Ping,Liu Yanling,Xia Lu,Wang Tianyun,Tian Qi,Li Ying,Hu Yiqiao,Zheng Yu,Jin Xuemin,Li Yunping,Xiong Wei,Tang Beisha,Feng Yong,Li Jiada,Pan Qian,Hu Zhengmao,Xia Kun

Publisher

Elsevier BV

Subject

Genetics (clinical)

Link

http://www.nature.com/articles/gim201528.pdf

Reference24 articles.

Cited by 61 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. Trio-based whole-exome sequencing reveals mutations in early-onset high myopia;BMJ Open Ophthalmology;2024-05

2. Collagen prolyl 4-hydroxylase isoenzymes I and II have sequence specificity towards different X-Pro-Gly triplets;Matrix Biology;2024-01

3. Whole-Exome Sequencing Among School-Aged Children With High Myopia;JAMA Network Open;2023-12-01

4. Association of TRMT2B gene variants with juvenile amyotrophic lateral sclerosis;Frontiers of Medicine;2023-10-24

5. CCDC66mutations are associated with high myopia through affected cell mitosis;Journal of Medical Genetics;2023-10-18

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