A genome-wide association study provides evidence for association of chromosome 8p23 (MYP10) and 10q21.1 (MYP15) with high myopia in the French population

Investigative Ophthalmology and Visual Science

Volumn 53, Issue 13, 2012, Pages 7983-7988

  Meng, Weihua ^a   Butterworth, Jacqueline ^b   Bradley, Declan T ^a   Hughes, Anne E ^a   Soler, Vincent ^c   Calvas, Patrick ^c   Malecaze, Francois ^c  

^a QUEEN'S UNIVERSITY BELFAST   (United Kingdom)

^b NEWCASTLE UNIVERSITY   (United Kingdom)

^c CHU PURPAN   (France)

Author keywords

[No Author keywords available]

Indexed keywords

METHIONINE SULFOXIDE REDUCTASE A; TANKYRASE;

ADULT; ARTICLE; COHORT ANALYSIS; CONTROLLED STUDY; FEMALE; GENE; GENE LOCUS; GENETIC ASSOCIATION; GENETIC SUSCEPTIBILITY; GENOME; GENOTYPING TECHNIQUE; HIGH MYOPIA; HUMAN; MAJOR CLINICAL STUDY; MALE; MYP10 GENE; MYP15 GENE; PRIORITY JOURNAL; QUALITY CONTROL; SINGLE NUCLEOTIDE POLYMORPHISM;

CHROMOSOMES, HUMAN, PAIR 10; CHROMOSOMES, HUMAN, PAIR 8; FEMALE; FRANCE; GENETIC PREDISPOSITION TO DISEASE; GENOME-WIDE ASSOCIATION STUDY; GENOTYPE; GENOTYPING TECHNIQUES; HUMANS; MALE; MIDDLE AGED; MYOPIA; MYOPIA, DEGENERATIVE; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 84873350228     PISSN: 01460404     EISSN: 15525783     Source Type: Journal    
DOI: 10.1167/iovs.12-10409     Document Type: Article

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