Incomplete congenital stationary night blindness associated with a novel variant in the CACNA1F gene.

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Bibliographic Details
Title: Incomplete congenital stationary night blindness associated with a novel variant in the CACNA1F gene.
Authors: Loo SP; Department of Ophthalmology, Royal Hospital for Children, NHS Greater Glasgow and Clyde, Glasgow, UK., Shipton C; Department of Ophthalmology, NHS Lanarkshire, Wishaw, UK., Hamilton M; West of Scotland Clinical Genetics Service, Queen Elizabeth University Hospital, NHS Greater Glasgow and Clyde, Glasgow, UK., Brown A; Department of Ophthalmology, NHS Lanarkshire, Wishaw, UK., Millar E; Department of Ophthalmology, Royal Hospital for Children, NHS Greater Glasgow and Clyde, Glasgow, UK., Malik I; Department of Medical Illustration, NHS Greater Glasgow and Clyde, Glasgow, UK., Craig M; Department of Medical Illustration, NHS Greater Glasgow and Clyde, Glasgow, UK., Hamilton R; Department of Clinical Physics and Bioengineering, Royal Hospital for Children, NHS Greater Glasgow and Clyde, Glasgow, UK. ruth.hamilton@glasgow.ac.uk.; College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, UK. ruth.hamilton@glasgow.ac.uk.
Source: Documenta ophthalmologica. Advances in ophthalmology [Doc Ophthalmol] 2026 Jun; Vol. 152 (3), pp. 401-407. Date of Electronic Publication: 2025 Nov 07.
Publication Type: Journal Article; Case Reports
Journal Info: Publisher: Kluwer Country of Publication: Netherlands NLM ID: 0370667 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1573-2622 (Electronic) Linking ISSN: 00124486 NLM ISO Abbreviation: Doc Ophthalmol Subsets: MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:1573-2622
DOI:10.1007/s10633-025-10062-x