Phenotypic Conservation in Patients With X-Linked Retinitis Pigmentosa Caused byRPGRMutations-Reference-Cited by-同舟云学术

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Phenotypic Conservation in Patients With X-Linked Retinitis Pigmentosa Caused byRPGRMutations

Published:2013-08-01 Issue:8 Volume:131 Page:1016
ISSN:2168-6165
Container-title:JAMA Ophthalmology
language:en
Short-container-title:JAMA Ophthalmol

Author:

Zahid Sarwar,Khan Naheed,Branham Kari,Othman Mohammad,Karoukis Athanasios J.,Sharma Nisha,Moncrief Ashley,Mahmood Mahdi N.,Sieving Paul A.,Swaroop Anand,Heckenlively John R.,Jayasundera Thiran

Publisher

American Medical Association (AMA)

Subject

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. Genetic Characteristics and Long-Term Follow-Up of Slovenian Patients with RPGR Retinal Dystrophy;International Journal of Molecular Sciences;2023-02-14

2. Retrospective Natural History Study of RPGR-Related Cone- and Cone-Rod Dystrophies While Expanding the Mutation Spectrum of the Disease;International Journal of Molecular Sciences;2022-06-28

3. Rare Co-Occurrence of Visual Snow in a Female Carrier With RPGRORF15-Associated Retinal Disorder;Frontiers in Genetics;2021-10-01

4. Genotype–Phenotype Analysis of RPGR Variations: Reporting of 62 Chinese Families and a Literature Review;Frontiers in Genetics;2021-06-23

5. Gene Therapy in X-linked Retinitis Pigmentosa Due to Defects in RPGR;International Ophthalmology Clinics;2021

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