Association of pattern dystrophy with an HTRA1 single-nucleotide polymorphism

Archives of Ophthalmology

Volumn 130, Issue 8, 2012, Pages 987-991

  Jaouni, Tareq ^a   Averbukh, Edward ^a   Burstyn Cohen, Tal ^b   Grunin, Michelle ^a   Banin, Eyal ^a   Sharon, Dror ^a   Chowers, Itay ^a  

^a HADASSAH HEBREW UNIVERSITY MEDICAL CENTER   (Israel)

^b HEBREW UNIVERSITY OF JERUSALEM   (Israel)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENT COMPONENT C3; COMPLEMENT FACTOR H; PERIPHERIN;

ADULT; ADULT ONSET FOVEOMACULAR VITELLIFORM DYSTROPHY; AGED; ALLELE; ARTICLE; BUTTERFLY SHAPED PIGMENT DYSTROPHY; FEMALE; GENE; GENETIC ASSOCIATION; GENETIC RISK; GENOTYPE; HTRA1 GENE; HUMAN; MAJOR CLINICAL STUDY; MALE; PIGMENT DISORDER; PREVALENCE; PRIORITY JOURNAL; RETINA DYSTROPHY; RETINA MACULA AGE RELATED DEGENERATION; SEQUENCE ANALYSIS; SINGLE NUCLEOTIDE POLYMORPHISM; VISUAL ACUITY;

AGED; AGED, 80 AND OVER; CHLORIDE CHANNELS; COMPLEMENT FACTOR H; CROSS-SECTIONAL STUDIES; EYE PROTEINS; FEMALE; FLUORESCEIN ANGIOGRAPHY; GENOTYPE; HUMANS; INTERMEDIATE FILAMENT PROTEINS; MALE; MEMBRANE GLYCOPROTEINS; MIDDLE AGED; NERVE TISSUE PROTEINS; PHENOTYPE; POLYMERASE CHAIN REACTION; POLYMORPHISM, SINGLE NUCLEOTIDE; RETINAL DYSTROPHIES; RISK FACTORS; SERINE ENDOPEPTIDASES; TOMOGRAPHY, OPTICAL COHERENCE; VITELLIFORM MACULAR DYSTROPHY;

EID: 84865574792     PISSN: 00039950     EISSN: 15383601     Source Type: Journal    
DOI: 10.1001/archophthalmol.2012.1483     Document Type: Article

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