Inherited retinal diseases in patients with ABCA4 gene mutations
Author:
Publisher
Media Sphere Publishing Group
Subject
Ophthalmology
Reference38 articles.
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3. Higgins CF. ABC transporters: from microorganisms to man . Annu Rev Cell Biol. 1992;8:67-113.
4. Screening ofABCA4Gene in a Chinese Cohort With Stargardt Disease or Cone-Rod Dystrophy With a Report on 85 Novel Mutations
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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. Morphological and functional indicators of retinal pigment epithelium and photoreceptor apparatus in inherited retinal diseases;Vestnik oftal'mologii;2020
2. Phenotype-genotype correlations in patients with inherited retinal diseases with p.G1961E mutation in the ABCA4 gene;Vestnik oftal'mologii;2019
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