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Article

Retinal Degeneration Secondary to MERTK Mutations: Potential Candidate for Gene Therapy.

International ophthalmology clinics - 1 Oct 2021

Shen-Sampas John H, Duret Stephanie, Duncan Jacque L

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Identifiers

PMID: 34584051
DOI: 10.1097/IIO.0000000000000374
PMCID: PMC8486302

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Retinal Degeneration Secondary to MERTK Mutations: Potential Candidate for Gene Therapy.PMID 34584051Read ↗

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A Comprehensive Review of Mutations in the MERTK Proto-Oncogene.Semantic proximity Read ↗

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Mutations in MERTK, the human orthologue of the RCS rat retinal dystrophy gene, cause retinitis pigmentosaSemantic proximity Read ↗

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