The gene for schnyder's crystalline corneal dystrophy maps to human chromosome 1p34.1-p36
Author:
Publisher
Oxford University Press (OUP)
Subject
Genetics (clinical),Genetics,Molecular Biology,General Medicine
Link
http://academic.oup.com/hmg/article-pdf/5/10/1667/1713289/5-10-1667.pdf
Cited by 52 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. Corneal Dysgeneses, Dystrophies, and Degenerations;Albert and Jakobiec's Principles and Practice of Ophthalmology;2022
2. Naturally occurring UBIAD1 mutations differentially affect menaquinone biosynthesis and vitamin K‐dependent carboxylation;The FEBS Journal;2021-12
3. Functional study of SCCD pathogenic gene UBIAD1 (Review);Molecular Medicine Reports;2021-08-06
4. Corneal Dysgeneses, Dystrophies, and Degenerations;Albert and Jakobiec's Principles and Practice of Ophthalmology;2021
5. Anterior segment optical coherence tomography for the diagnosis of corneal dystrophies according to the IC3D classification;Survey of Ophthalmology;2018-05
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