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Article

X-linked cone dystrophy with an uncommon tapetal-like sheen caused by a novel RPGR variant.

Canadian journal of ophthalmology. Journal canadien d'ophtalmologie - 1 Jun 2024

Zhai Yi, Wright Tom, Ballios Brian G

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Topics

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Share to DNA Mutational Analysis
Share to Electroretinography
Share to Eye Proteins
Share to Genetic Diseases, X-Linked

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Retinal Cone Photoreceptor Cells

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Source

Identifiers

PMID: 38128582
DOI: 10.1016/j.jcjo.2023.11.016

Genes

RPGR

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

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