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Volumn 26, Issue 3, 2000, Pages 270-271
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Mutations in MERTK, the human orthologue of the RCS rat retinal dystrophy gene, cause retinitis pigmentosa
a
a
b
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a
d
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c
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Author keywords
[No Author keywords available]
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Indexed keywords
COMPLEMENTARY DNA;
MICROSATELLITE DNA;
ARTICLE;
CHROMOSOME 2Q;
DNA DETERMINATION;
DNA SEQUENCE;
GENE DELETION;
GENOME;
HUMAN;
INTRON;
NONHUMAN;
PHOTORECEPTOR;
PRIORITY JOURNAL;
RAT;
RETINA DYSTROPHY;
RETINITIS PIGMENTOSA;
SEQUENCE ANALYSIS;
ADULT;
AMINO ACID SUBSTITUTION;
ANIMALS;
CHROMOSOMES, HUMAN, PAIR 2;
CLONING, MOLECULAR;
CODON;
CONSANGUINITY;
DISEASE MODELS, ANIMAL;
DNA MUTATIONAL ANALYSIS;
EXONS;
EYE PROTEINS;
FEMALE;
FRAMESHIFT MUTATION;
GENES, RECESSIVE;
HUMANS;
INTRONS;
MALE;
MIDDLE AGED;
MUTATION, MISSENSE;
PHAGOCYTOSIS;
POINT MUTATION;
POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL;
PROTO-ONCOGENE PROTEINS;
RATS;
RATS, INBRED STRAINS;
RECEPTOR PROTEIN-TYROSINE KINASES;
RETINAL DEGENERATION;
RETINITIS PIGMENTOSA;
RNA SPLICE SITES;
ROD OUTER SEGMENTS;
RODENT DISEASES;
SEQUENCE DELETION;
SPECIES SPECIFICITY;
TERMINATOR REGIONS (GENETICS);
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EID: 0033757463
PISSN: 10614036
EISSN: None
Source Type: Journal
DOI: 10.1038/81555 Document Type: Article |
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Times cited : (585)
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References (15)
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