Clinical and Genetic Identification of a Large Chinese Family with Autosomal Dominant Retinitis Pigmentosa-Reference-Cited by-同舟云学术

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Clinical and Genetic Identification of a Large Chinese Family with Autosomal Dominant Retinitis Pigmentosa

Published:2013-07-08 Issue:1 Volume:36 Page:64-69
ISSN:1381-6810
Container-title:Ophthalmic Genetics
language:en
Short-container-title:Ophthalmic Genetics

Author:

Yang Yezhen,Tian Di,Lee Janet,Zeng Jing,Zhang Huiming,Chen Siying,Guo Hui,Xiong Zhiming,Xia Kun,Hu Zhengmao,Luo Jing

Publisher

Informa UK Limited

Subject

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

Link

http://www.tandfonline.com/doi/pdf/10.3109/13816810.2013.809458

Reference31 articles.

1. Retinitis pigmentosa

2. Prevalence of Retinitis Pigmentosa in Urban and Rural Adult Chinese: The Beijing Eye Study

3. Perspective on Genes and Mutations Causing Retinitis Pigmentosa

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1. Clinical and Genetic Findings in a Cohort of Patients with PRPF31-Associated Retinal Dystrophy;American Journal of Ophthalmology;2024-11

2. Clinical characterization of patients with PRPF31 -related retinitis pigmentosa and asymptomatic carriers: a cross-sectional study;Ophthalmic Genetics;2023-06-09

3. Clinical Evidence for the Importance of the Wild-Type PRPF31 Allele in the Phenotypic Expression of RP11;Genes;2021-06-14

4. Exploring microperimetry and autofluorescence endpoints for monitoring disease progression in PRPF31-associated retinopathy;Ophthalmic Genetics;2020-09-27

5. Mutation spectrum of PRPF31, genotype-phenotype correlation in retinitis pigmentosa, and opportunities for therapy;Experimental Eye Research;2020-03

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