Clinical studies of X-linked retinitis pigmentosa in three Swedish families with newly identified mutations in the RP2 and RPGR-ORF15 genes-Reference-Cited by-同舟云学术

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Clinical studies of X-linked retinitis pigmentosa in three Swedish families with newly identified mutations in the RP2 and RPGR-ORF15 genes

Published:2003-01 Issue:4 Volume:24 Page:215-223
ISSN:1381-6810
Container-title:Ophthalmic Genetics
language:en
Short-container-title:Ophthalmic Genetics

Author:

Andréasson Sten,Breuer Debra K.,Eksandh Louise,Ponjavic Vesna,Frennesson Christina,Hiriyanna Suja,Filippova Elena,Yashar Beverly M.,Swaroop Anand

Publisher

Swets & Zeitlinger Publishers

Subject

Genetics (clinical),Ophthalmology,Pediatrics, Perinatology and Child Health

Link

http://www.tandfonline.com/doi/pdf/10.1076/opge.24.4.215.17228

Reference27 articles.

1. X-linked retinitis pigmentosa.

2. Close genetic linkage between X-linked retinitis pigmentosa and a restriction fragment length polymorphism identified by recombinant DNA probe L1.28

Cited by 25 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. From onset to blindness: a comprehensive analysis ofRPGR-associated X-linked retinopathy in a large cohort in China;Journal of Medical Genetics;2024-08-17

2. Early Macular Involvement in Non-syndromic Retinitis Pigmentosa;Macular Diseases - An Update [Working Title];2023-12-06

3. Retinitis pigmentosa GTPase regulator-related retinopathy and gene therapy;Saudi Journal of Ophthalmology;2023-10

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

5. Impaired glutamylation of RPGR ^ORF15 underlies the cone-dominated phenotype associated with truncating distal ORF15 variants;Proceedings of the National Academy of Sciences;2022-11-29

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