Phenotype-genotype correlations in patients with inherited retinal diseases with p.G1961E mutation in the ABCA4 gene-Reference-Cited by-同舟云学术

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Phenotype-genotype correlations in patients with inherited retinal diseases with p.G1961E mutation in the ABCA4 gene

Published:2019 Issue:4 Volume:135 Page:10
ISSN:0042-465X
Container-title:Vestnik oftal'mologii
language:en
Short-container-title:Vestn. oftal'mol.

Author:

Sheremet N. L.,Grushke I. G.,Zhorzholadze N. V.,Ronzina I. A.,Mikaelyan A. A.,Kadyshev V. V.,Tanas A. S.,Anoshkin K. I.,Strelnikov V. V.

Publisher

Media Sphere Publishing Group

Subject

Ophthalmology

Reference22 articles.

1. Mutation Spectrum of the ABCA4 Gene in 335 Stargardt Disease Patients From a Multicenter German Cohort—Impact of Selected Deep Intronic Variants and Common SNPs

2. Inherited retinal diseases in patients with ABCA4 gene mutations

3. van Driel MA, Maugeri A, Klevering BJ, Hoyng CB, Cremers FP. ABCR unites what ophthalmologists divide (s). Ophthalmic genetics. 1998;19(3):117-122.

4. Molecular genetic diagnosis of Stargardt disease

5. In SilicoFunctional Meta-Analysis of 5,962ABCA4Variants in 3,928 Retinal Dystrophy Cases

Cited by 2 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. Inactive macular neovascularization in Stargardt’s disease;Ophthalmology Reports;2023-10-17

2. Current Management of Inherited Retinal Degeneration Patients in Europe: Results of a 2-Year Follow-Up Multinational Survey by the European Vision Institute Clinical Research Network – EVICR.net;Ophthalmic Research;2023

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