Complement factor H 402H variant and reticular macular disease

Archives of Ophthalmology

Volumn 129, Issue 8, 2011, Pages 1061-1066

  Smith, R Theodore ^a,b   Merriam, Joanna E ^a   Sohrab, Mahsa A ^a   Pumariega, Nicole M ^a,b   Barile, Gaetano ^a   Blonska, Anna M ^a   Haans, Raymond ^a   Madigan, David ^c   Allikmets, Rando ^a,d  

^a New York Presbyterian Hospital   (United States)

^b NONE   (United States)

^c Och Spine at New York Presbyterian Hospitals   (United States)

^d NewYork Presbyterian Hospital   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENT FACTOR H;

402H GENE; ADULT; AGED; ALLELE; ARTICLE; CONFIDENCE INTERVAL; CONTROLLED STUDY; DISEASE ASSOCIATION; FEMALE; GENE; HOMOZYGOSITY; HUMAN; HYPERTENSION; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; RETINA MACULA AGE RELATED DEGENERATION; RETINA MACULOPATHY; RISK;

AGED; AGED, 80 AND OVER; COMPLEMENT FACTOR H; FEMALE; GENE FREQUENCY; GENOTYPE; HUMANS; MACULAR DEGENERATION; MALE; MICROSCOPY, CONFOCAL; ODDS RATIO; PHENOTYPE; POLYMERASE CHAIN REACTION; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH; POLYMORPHISM, SINGLE NUCLEOTIDE; PROTEINS; RISK FACTORS; TOMOGRAPHY, OPTICAL COHERENCE;

EID: 80051559056     PISSN: 00039950     EISSN: 15383601     Source Type: Journal    
DOI: 10.1001/archophthalmol.2011.212     Document Type: Article

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