Best’s vitelliform macular dystrophy caused by a new mutation (Val89Ala) in the VMD2 gene-Reference-Cited by-同舟云学术

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Best’s vitelliform macular dystrophy caused by a new mutation (Val89Ala) in the VMD2 gene

Published:2001-01 Issue:2 Volume:22 Page:107-115
ISSN:1381-6810
Container-title:Ophthalmic Genetics
language:en
Short-container-title:Ophthalmic Genetics

Author:

Eksandh Louise,Bakall Benjamin,Bauer Birgitta,Wadelius Claes,Andréasson Sten

Publisher

Swets & Zeitlinger Publishers

Subject

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

Link

http://www.tandfonline.com/doi/pdf/10.1076/opge.22.2.107.2226

Reference19 articles.

1. Long-term Evaluation of Patients with Best's Vitelliform Dystrophy

2. Hereditary Vitelline Macular Degeneration

Cited by 33 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. Impaired Bestrophin Channel Activity in an iPSC-RPE Model of Best Vitelliform Macular Dystrophy (BVMD) from an Early Onset Patient Carrying the P77S Dominant Mutation;International Journal of Molecular Sciences;2022-07-04

2. Vitelliform Macular Dystrophy;Inherited Retinal Disease;2022

3. Full‐field electroretinography in age‐related macular degeneration: an overall retinal response;Acta Ophthalmologica;2020-08-24

4. Clinical Genetics of Vitelliform Macular Dystrophy: An Asian Perspective;Essentials in Ophthalmology;2018-11-04

5. Novel Presenting Phenotype in a Child With Autosomal Dominant Best's Vitelliform Macular Dystrophy;Ophthalmic Surgery, Lasers and Imaging Retina;2017-07

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