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Article

Prph2 mutations as a cause of electronegative ERG.

Retina (Philadelphia, Pa.) - 1 Jun 2014

Ba-Abbad Rola, Robson Anthony G, Yap Yew C, Moore Anthony T, Webster Andrew R, Holder Graham E

Abstract excerpt

PURPOSE: To describe the phenotypic and genotypic features in patients with PRPH2 mutations and negative electroretinograms. METHODS: Retrospective observational case series. Records of patients with a confirmed molecular diagnosis of PRPH2 mutation, and an electronegative electroretinogram (redu...

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Source

Identifiers

PMID: 24608669
DOI: 10.1097/IAE.0000000000000052

Genes

PRPH2
ERG

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-24608669-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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