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Article

Novel PRPF31 mutations associated with Chinese autosomal dominant retinitis pigmentosa patients.

Molecular vision - 1 Jan 2012

Xu Fei, Sui Ruifang, Liang Xiaofang, Li Hui, Jiang Ruxin, Dong Fangtian

Abstract excerpt

PURPOSE: To identify the mutations in the pre-mRNA processing factor 31 homolog (PRPF31) gene in Chinese families with autosomal dominant retinitis pigmentosa (adRP) and to characterize the clinical features of those patients who were found to have mutations in the PRPF31 gene. METHODS: Detailed...

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Source

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Identifiers

PMID: 23288994
PMCID: PMC3534138

Genes

PRPF31

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-23288994-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

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

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