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Article

Human iPSC derived disease model of MERTK-associated retinitis pigmentosa.

Scientific reports - 11 Aug 2015

Lukovic Dunja, Artero Castro Ana, Delgado Ana Belen Garcia, Bernal María de los Angeles Martín, Luna Pelaez Noelia, Díez Lloret Andrea, Perez Espejo Rocío, Kamenarova Kunka, Fernández Sánchez Laura, Cuenca Nicolás, Cortón Marta, Avila Fernandez Almudena, Sorkio Anni, Skottman Heli, Ayuso Carmen, Erceg Slaven, Bhattacharya Shomi S

Abstract excerpt

Retinitis pigmentosa (RP) represents a genetically heterogeneous group of retinal dystrophies affecting mainly the rod photoreceptors and in some instances also the retinal pigment epithelium (RPE) cells of the retina. Clinical symptoms and disease progression leading to moderate to severe loss of vision are well established and despite significant progress in the identification of causative genes, the disease...

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Source

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Identifiers

PMID: 26263531
DOI: 10.1038/srep12910
PMCID: PMC4531787

Genes

MERTK
RPE

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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