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Ophthalmic Genetics, ISSN 1381-6810, 03/2019, Volume 40, Issue 2, pp. 170 - 176
Background: Retinitis pigmentosa (RP) is a clinically and genetically heterogeneous disease causing progressive degeneration of retinal photoreceptor cells.... 
hereditary X-linked recessive diseases | X-linked carrier | Retinitis pigmentosa | X-linked retinal disease | RPGR
Journal Article
Investigative Ophthalmology and Visual Science, ISSN 0146-0404, 2010, Volume 51, Issue 8, pp. 4266 - 4272
Journal Article
Investigative Ophthalmology & Visual Science, ISSN 0146-0404, 04/2010, Volume 51, Issue 4, pp. 2236 - 2242
Journal Article
Molecular Vision, ISSN 1090-0535, 2011, Volume 17, Issue 325-26, pp. 3013 - 3024
Journal Article
International Journal of Neuroscience, ISSN 0020-7454, 1/2015, Volume 125, Issue 1, pp. 43 - 49
Journal Article
Investigative Ophthalmology & Visual Science, ISSN 0146-0404, 09/2009, Volume 50, Issue 9, pp. 4065 - 4071
Journal Article
Nature Genetics, ISSN 1061-4036, 11/2000, Volume 26, Issue 3, pp. 270 - 271
Mutation of a receptor tyrosine kinase gene, Mertk, in the Royal College of Surgeons (RCS) rat results in defective phagocytosis of photoreceptor outer... 
EPITHELIUM | C-MER | PROTOONCOGENE | GENETICS & HEREDITY | Sequence Deletion | Frameshift Mutation | Species Specificity | Humans | Middle Aged | Male | Terminator Regions, Genetic - genetics | Mutation, Missense | Polymorphism, Single-Stranded Conformational | Chromosomes, Human, Pair 2 - genetics | Rodent Diseases - genetics | DNA Mutational Analysis | c-Mer Tyrosine Kinase | Cloning, Molecular | Rod Cell Outer Segment - pathology | Adult | Female | Proto-Oncogene Proteins | Codon - genetics | Eye Proteins - genetics | Disease Models, Animal | Receptor Protein-Tyrosine Kinases - deficiency | Rodent Diseases - enzymology | Introns - genetics | RNA Splice Sites - genetics | Retinal Degeneration - genetics | Rats | Retinitis Pigmentosa - genetics | Exons - genetics | Genes, Recessive | Point Mutation | Retinitis Pigmentosa - enzymology | Animals | Rats, Inbred Strains - genetics | Receptor Protein-Tyrosine Kinases - genetics | Consanguinity | Retinal Degeneration - pathology | Retinal Degeneration - enzymology | Retinal Degeneration - veterinary | Phagocytosis | Amino Acid Substitution | Complications and side effects | Care and treatment | Gene mutations | Retinitis pigmentosa | Retinal degeneration | Causes of | Genetic aspects | Research | Identification and classification | Health aspects | chromosome 2 | MERTK gene | Index Medicus
Journal Article
Nature Genetics, ISSN 1061-4036, 1998, Volume 18, Issue 1, pp. 11 - 12
Retinitis pigmentosa (RP) denotes a group of inherited eye disorders characterized by loss of rod photoreceptor function, leading to a progressive degeneration... 
GENETICS & HEREDITY | Homozygote | Frameshift Mutation | ATP-Binding Cassette Transporters - genetics | Macular Degeneration - genetics | Pedigree | Humans | Retinitis Pigmentosa - genetics | Female | Male | Genes, Recessive
Journal Article
Journal Article