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