数据链接：
官方服务：
资源简介：
(XLSX)
应用场景：
创建时间：
2018-01-06
相关数据集
Additional file 2 of Novel variants of ABCA4 in Han Chinese families with Stargardt disease
Additional file 2: Table S2. Twenty-one ABCA4 variants identified in this study and their in silico functional assessment.
DataCite Commons2024-02-07 更新150
Unusual clinical phenotype of Stargardt disease
ABSTRACT Mutations in the ABCA4 gene are a common cause of Stargardt disease; however, other retinal phenotypes have also been associated with mutations in this gene. We describe an observational case
DataCite Commons2022-05-30 更新80
Supplementary Material for: Colour Vision in Stargardt Disease
Purpose: To investigate the type and severity of acquired colour vision deficiencies (CVDs) in molecularly proven Stargardt disease (STD) and to establish whether a relationship exists between best-co
NIAID Data Ecosystem60
Supplementary Material for: Colour Vision in Stargardt Disease
Purpose: To investigate the type and severity of acquired colour vision deficiencies (CVDs) in molecularly proven Stargardt disease (STD) and to establish whether a relationship exists b
DataCite Commons2020-09-02 更新90
Clinical and electroretinographic profile of 27 patients with Stargardt disease treated at a hospital in Brazil
ABSTRACT Purpose: Stargardt disease is the most common type of juvenile-onset macular dystrophy. It is bilateral and symmetrical in appearance, affects the macula, and its main characteristic is the l
DataCite Commons2022-05-30 更新80
