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Article

Retinitis pigmentosa: mutations in a receptor tyrosine kinase gene, MERTK.

Journal of biosciences - 1 Mar 2001

Kumar A

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Share to c-Mer Tyrosine Kinase
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 11255506
DOI: 10.1007/BF02708973

Genes

MERTK

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

Retinitis pigmentosa: mutations in a receptor tyrosine kinase gene, MERTK.PMID 11255506Read ↗

Retinal Degeneration Secondary to MERTK Mutations: Potential Candidate for Gene Therapy.Semantic proximity Read ↗

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

MERTK missense variants in three patients with retinitis pigmentosa.Semantic proximity Read ↗

MERTK mutation update in inherited retinal diseases.Semantic proximity Read ↗

Clinical characterisation of a family with retinal dystrophy caused by mutation in the Mertk gene.Semantic proximity Read ↗

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

Screening of the MERTK gene for mutations in Japanese patients with autosomal recessive retinitis pigmentosa.Semantic proximity Read ↗

Homozygous mutation in MERTK causes severe autosomal recessive retinitis pigmentosa.Semantic proximity Read ↗

A novel MERTK mutation causing retinitis pigmentosa.Semantic proximity Read ↗

Bi-Allelic Pathogenic Variations in MERTK Including Deletions Are Associated with an Early Onset Progressive Form of Retinitis Pigmentosa.Semantic proximity Read ↗

Novel splice donor site mutation in MERTK gene associated with retinitis pigmentosa.Semantic proximity Read ↗

MERTK arginine-844-cysteine in a patient with severe rod-cone dystrophy: loss of mutant protein function in transfected cells.Semantic proximity Read ↗

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