Acta Ophthalmol

A genetic and historical perspective on the origins of keratitis fugax hereditaria.

Immonen AT, Luostarinen SP, Lahermo P, ..., Backlund MP, Turunen JA

Acta Ophthalmol - (-) - [2026-09-16; online 2026-09-16]

NGI SNP genotyping [Service] NGI Uppsala (SNP&SEQ Technology Platform) [Service] National Genomics Infrastructure [Service]

The value of age of onset and family history as predictors of molecular diagnosis in a Swedish cohort of inherited retinal disease.

De Geer K, Löfgren S, Lindstrand A, Kvarnung M, Björck E

Acta Ophthalmol 103 (3) 327-338 [2025-05-00; online 2024-12-06]

Clinical Genomics [Service] Clinical Genomics Stockholm [Service]

TCF4 trinucleotide repeat expansion in Swedish cases with Fuchs' endothelial corneal dystrophy.

Viberg A, Westin IM, Golovleva I, Byström B

Acta Ophthalmol 100 (5) 541-548 [2022-08-00; online 2021-10-13]

Clinical Genomics [Service] Clinical Genomics Umeå [Service]