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Article

Genetic and bioinformatic analysis of RHO and PRPH2 variants in north Indian retinitis pigmentosa patients.

Japanese journal of ophthalmology - 1 Mar 2026

Bhardwaj Aarti, Phogat Jitender, Yadav Manoj, Yadav Anshu, Panghal Vishal, Singh Mayank, Sharma Sapna, Kumar Rakesh, Tanwar Mukesh

Abstract excerpt

PURPOSE: Retinitis Pigmentosa (RP) represents the most common form of inherited retinal dystrophy (IRD), identified by a gradual degeneration of photoreceptors, ultimately resulting in nyctalopia and impaired vision. This study was conducted to screen the rhodopsin and peripherin2 genes for possible pathogenic mutations in north Indian RP patients. STUDY DESIGN: We focused on assessing the whole coding region and...

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Identifiers

PMID: 40880019
DOI: 10.1007/s10384-025-01262-8

Genes

PRPH2
RHO

Variants

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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