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Article

Investigating the mechanism of disease in the RP10 form of retinitis pigmentosa.

Advances in experimental medicine and biology - 1 Jan 2010

Spellicy Catherine J, Xu Dong, Cobb Garrett, Hedstrom Lizbeth, Bowne Sara J, Sullivan Lori S, Daiger Stephen P

Abstract excerpt

Retinitis pigmentosa (RP) is a disease characterized by its vast heterogeneity. Many genes are associated with RP, and the disease causing mutations identified in these genes are even more numerous. To date there are 15 genes that cause autosomal dominant RP (adRP) alone. The role of some of these genes, while complex and not completely understood, is somewhat intuitive in that they are involved in pathways such...

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Source

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Identifiers

PMID: 20238057
DOI: 10.1007/978-1-4419-1399-9_62
PMCID: PMC4113320

Genes

IMPDH1

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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