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Article

PRPF31 alternative splicing and expression in human retina.

Ophthalmic genetics - 1 Jun 2009

Tanackovic Goranka, Rivolta Carlo

Abstract excerpt

PURPOSE: To provide a mechanistic link between mutations in PRPF31, and essential and ubiquitously expressed gene, and retinitis pigmentosa, a disorder restricted to the eye. METHODS: We investigated the existence of retina-specific PRPF31 isoforms and the expression of this gene in human retina and other tissues, as well as in cultured human cell lines. PRPF31 transcripts were examined by RT-PCR, quantitative...

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Source

Identifiers

PMID: 19373678
DOI: 10.1080/13816810902744621

Genes

PRPF31

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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