Whole Exome Sequencing Reveals GUCY2D as a Major Gene Associated With Cone and Cone-Rod Dystrophy in Israel-Reference-Cited by-同舟云学术

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Whole Exome Sequencing Reveals GUCY2D as a Major Gene Associated With Cone and Cone-Rod Dystrophy in Israel

Published:2014-12-16 Issue:1 Volume:56 Page:420-430
ISSN:0146-0404
Container-title:Investigative Ophthalmology & Visual Science
language:en
Short-container-title:Investigative Ophthalmology & Visual Science

Author:

Lazar C. H.,Mutsuddi M.,Kimchi A.,Zelinger L.,Mizrahi-Meissonnier L.,Marks-Ohana D.,Boleda A.,Ratnapriya R.,Sharon D.,Swaroop A.,Banin E.

Publisher

Association for Research in Vision and Ophthalmology (ARVO)

Subject

Cellular and Molecular Neuroscience,Sensory Systems,Ophthalmology

Cited by 30 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. Disruption of CFAP418 interaction with lipids causes widespread abnormal membrane-associated cellular processes in retinal degenerations;JCI Insight;2024-01-09

2. A natural history study of autosomal dominant GUCY2D-associated cone–rod dystrophy;Documenta Ophthalmologica;2023-09-29

3. Occult Macular Dysfunction Syndrome: Identification of Multiple Pathologies in a Clinical Spectrum of Macular Dysfunction with Normal Fundus in East Asian Patients: EAOMD Report No. 5;Genes;2023-09-26

4. Genes y Mutaciones Implicados en Distrofias Retinianas;Revista Oftálmica;2023-07-15

5. Interactions between C8orf37 and FAM161A, Two Ciliary Proteins Essential for Photoreceptor Survival;International Journal of Molecular Sciences;2022-10-10

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