Autosomal dominant pigmented paravenous retinochoroidal atrophy associated with pathogenic variant in HK1 gene

Graefes Arch Clin Exp Ophthalmol. 2026 Jan 16. doi: 10.1007/s00417-025-07107-x. Online ahead of print.
No abstract available

Keywords: Fundus autofluorescence; HK1; Hexokinase 1; PPRCA; Pigmented paravenous retinochoroidal atrophy.