Novel rhodopsin mutation in a Chinese family with autosomal dominant retinitis pigmentosa

Ophthalmic Genetics

Volumn 22, Issue 3, 2001, Pages 155-162

  Zhao, Kanxing ^a   Xiong, Shihong ^a   Wang, Li ^a   Wang, Lejin ^a   Cui, Yun ^a   Wang, Qing ^a  

^a LERNER RESEARCH INSTITUTE   (United States)

Author keywords

Genetic disease; Mutation; Retinal degeneration; Retinal dystrophy; Retinitis pigmentosa; Rhodopsin (RHO)

Indexed keywords

MUTANT PROTEIN; RHODOPSIN;

ADULT; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CHINESE; CODON; CONTROLLED STUDY; DNA SEQUENCE; EUROPE; FAMILY STUDY; FEMALE; GENE IDENTIFICATION; GENE LOCUS; GENE MUTATION; GENETIC CODE; GENOME ANALYSIS; HUMAN; INTRON; MAJOR CLINICAL STUDY; MALE; NIGHT BLINDNESS; NORTH AMERICA; OPTIC NERVE ATROPHY; PIGMENTATION; PREVALENCE; PRIORITY JOURNAL; RACE DIFFERENCE; RETINA CONE; RETINA ROD; RETINITIS PIGMENTOSA; SINGLE STRAND CONFORMATION POLYMORPHISM; VISUAL ACUITY; VISUAL FIELD;

ADULT; AMINO ACID SEQUENCE; BASE SEQUENCE; CHINA; CODON, TERMINATOR; DNA PRIMERS; FEMALE; HUMANS; MALE; MIDDLE AGED; MOLECULAR SEQUENCE DATA; MUTATION; PEDIGREE; POLYMERASE CHAIN REACTION; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; RETINITIS PIGMENTOSA; RHODOPSIN; SEQUENCE ANALYSIS, DNA; X CHROMOSOME;

EID: 0035574104     PISSN: 13816810     EISSN: None     Source Type: Journal    
DOI: 10.1076/opge.22.3.155.2225     Document Type: Article

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