Spectrum of color gene deletions and phenotype in patients with blue cone monochromacy-Reference-Cited by-同舟云学术

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Spectrum of color gene deletions and phenotype in patients with blue cone monochromacy

Published:2000-07 Issue:1 Volume:107 Page:75-82
ISSN:0340-6717
Container-title:Human Genetics
language:en
Short-container-title:Hum Genet

Author:

Ayyagari Radha,Kakuk Laura E.,Bingham Eve L.,Szczesny Janet J.,Kemp Jennifer,Toda Yumiko,Felius Joost,Sieving Paul A.

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s004390000338.pdf

Cited by 22 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. Screening copy number variations in 35 unsolved inherited retinal disease families;Human Genetics;2024-01-29

2. Screening Copy Number Variations in 35 unsolved Inherited Retinal Disease Families;2023-09-18

3. Color Vision in Blue Cone Monochromacy: Outcome Measures for a Clinical Trial;Translational Vision Science & Technology;2023-01-24

4. The landscape of submicroscopic structural variants at the OPN1LW/OPN1MW gene cluster on Xq28 underlying blue cone monochromacy;Proceedings of the National Academy of Sciences;2022-06-27

5. Promises and pitfalls of evaluating photoreceptor-based retinal disease with adaptive optics scanning light ophthalmoscopy (AOSLO);Progress in Retinal and Eye Research;2021-07

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