Homozygous initiation codon-altering complex variant causes rapid-onset chorioretinopathy phenotype in ABCA4 disease

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Authors: Naeem Sbaiti, Maximilian D. Kong, Johnathan Bailey, Abdhel Exinor, Stephen H. Tsang
Cited by: 0
References: 26

Fields of Study & Subjects

Retinal Development and Disorders Retinal Diseases and Treatments Lysosomal Storage Disorders Research

Publication details

Journal / source
Documenta Ophthalmologica
Volume
153
Issue
1
Pages
115–121
Publication date
13 January 2026
Language
EN