A variant form of Oguchi disease mapped to 13q34 associated with partial deletion of GRK1 gene

Molecular Vision

Volumn 11, Issue , 2005, Pages 977-985

  Zhang, Qingjiong ^a,c   Zulfiqar, Fareeha ^b   Riazuddin, S Amer ^a,b   Xiao, Xueshan ^a,c   Yasmeen, Afshan ^b   Rogan, Peter K ^d   Caruso, Raphael ^a   Sieving, Paul A ^a   Riazuddin, Sheikh ^b   Hejtmancik, J Fielding ^a  

^a NATIONAL EYE INSTITUTE   (United States)

^b UNIVERSITY OF THE PUNJAB   (Pakistan)

^c SUN YAT SEN UNIVERSITY   (China)

^d UNIVERSITY OF MISSOURI KANSAS CITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

DEOXYRIBONUCLEOTIDE; G PROTEIN COUPLED RECEPTOR KINASE; G PROTEIN COUPLED RECEPTOR KINASE 1; UNCLASSIFIED DRUG; VISUAL PIGMENT;

ACTION POTENTIAL; ADOLESCENT; ADULT; ARTICLE; CALCULATION; CHILDHOOD DISEASE; CHROMOSOME 13Q; CLINICAL ARTICLE; CLINICAL FEATURE; CONTROLLED STUDY; DARK ADAPTATION; ELECTRORETINOGRAPHY; EXON; EYE FUNDUS; EYE PHOTOGRAPHY; FAMILIAL DISEASE; GENE DELETION; GENE LOCUS; GENE MAPPING; GENE MUTATION; GENE SEGREGATION; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENETIC LINKAGE; GENETIC SCREENING; GENETIC VARIABILITY; GENOME ANALYSIS; HAPLOTYPE; HUMAN; MICROSATELLITE MARKER; NIGHT BLINDNESS; NUCLEOTIDE SEQUENCE; OGUCHI DISEASE; PAKISTAN; PHENOMENOLOGY; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RECORDING; RETINA BLOOD VESSEL; RETINA CONE; RETINA DEGENERATION; RETINA DISEASE; RETINA ROD; RETINITIS PIGMENTOSA; SCORING SYSTEM; SEQUENCE ANALYSIS; VISUAL ACUITY; VISUAL SYSTEM EXAMINATION;

ADOLESCENT; ADULT; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 13; CONSANGUINITY; DARK ADAPTATION; ELECTRORETINOGRAPHY; EXONS; FEMALE; GENE DELETION; HUMANS; LINKAGE (GENETICS); LOD SCORE; MALE; NIGHT BLINDNESS; PAKISTAN; PEDIGREE; POLYMERASE CHAIN REACTION; RETINA; RETINAL DISEASES; RHODOPSIN KINASE;

EID: 28044461491     PISSN: 10900535     EISSN: 10900535     Source Type: Journal    
DOI: None     Document Type: Article

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