Exfoliation syndrome and exfoliation glaucoma-associated LOXL1 variations are not involved in pigment dispersion syndrome and pigmentary glaucoma

Molecular Vision

Volumn 14, Issue , 2008, Pages 1254-1262

  Rao, Kollu Nageswara ^a   Ritch, Robert ^b   Dorairaj, Syril K ^b,c   Kaur, Inderjeet ^a   Liebmann, Jeffrey M ^b   Thomas, Ravi ^a,d   Chakrabarti, Subhabrata ^a  

^a L V PRASAD EYE INSTITUTE   (India)

^b NEW YORK EYE AND EAR INFIRMARY   (United States)

^c BETH ISRAEL MEDICAL CENTER   (United States)

^d QUEENSLAND EYE INSTITUTE   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

GENE PRODUCT; LYSYL OXIDASE LIKE 1 PROTEIN;

ARTICLE; CAUCASIAN; CLOSED ANGLE GLAUCOMA; COHORT ANALYSIS; COMPUTER PROGRAM; CONTROLLED STUDY; DIAGNOSTIC IMAGING; EXFOLIATION SYNDROME; GENE FREQUENCY; GENE LINKAGE DISEQUILIBRIUM; GENE LOCUS; GENE SEQUENCE; GENETIC ALGORITHM; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENETIC IDENTIFICATION; GENETIC SCREENING; GENETIC VARIABILITY; GENOTYPE; GLAUCOMA; HAPLOTYPE; HUMAN; MAJOR CLINICAL STUDY; OPEN ANGLE GLAUCOMA; PATHOGENESIS; PHENOTYPE; PIGMENT DISORDER; PIGMENT GLAUCOMA; POLYMERASE CHAIN REACTION; PRIMARY GLAUCOMA; PRIORITY JOURNAL; PROMOTER REGION; PUPILLOGRAPHY; SINGLE NUCLEOTIDE POLYMORPHISM;

AMINO ACID OXIDOREDUCTASES; CASE-CONTROL STUDIES; EXFOLIATION SYNDROME; GENE FREQUENCY; GENETIC PREDISPOSITION TO DISEASE; GLAUCOMA, OPEN-ANGLE; HAPLOTYPES; HUMANS; PIGMENTATION DISORDERS; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 48949116403     PISSN: None     EISSN: 10900535     Source Type: Journal    
DOI: None     Document Type: Article

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