Genetic associations of common deletion polymorphisms in families with Avellino corneal dystrophy

Biochemical and Biophysical Research Communications

Volumn 387, Issue 4, 2009, Pages 688-693

  Park, Miey ^a   Kim, Dong Joon ^a   Kim, Kwang Joong ^a,b   Hong, Chang Bum ^a   Kim, Young Jin ^a   Cheong, Hyun Sub ^c   Shin, Hyoung Doo ^d   Lee, Eun Ju ^e   Kim, Han Na ^e   Chung, Hye Won ^e   Kim, Eung Kweon ^f   Lee, Jong Young ^a   Kim, Hyung Lae ^a  

^a Korea National Institute of Health   (South Korea)

^b Kangwon National University   (South Korea)

^c SNP Genetics Inc   (South Korea)

^d Sogang University   (South Korea)

^e Ewha Womans University School of Medicine   (South Korea)

^f Yonsei University College of Medicine   (South Korea)

Author keywords

Avellino corneal dystrophy (ACD); Copy number variation; Deletion polymorphism; HLA F gene

Indexed keywords

HLA F ANTIGEN;

ADULT; ARTICLE; AVELLINO CORNEAL DYSTROPHY; CASE CONTROL STUDY; CONGENITAL CORNEA DYSTROPHY; FEMALE; GENE; GENE DELETION; GENE LINKAGE DISEQUILIBRIUM; GENETIC ASSOCIATION; GENETIC RISK; GENOTYPE; HLA F GENE; HUMAN; MAJOR CLINICAL STUDY; MALE; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM;

CORNEAL DYSTROPHIES, HEREDITARY; GENETIC PREDISPOSITION TO DISEASE; GENOME-WIDE ASSOCIATION STUDY; HUMANS; KOREA; LINKAGE DISEQUILIBRIUM; PEDIGREE; POLYMORPHISM, SINGLE NUCLEOTIDE; SEQUENCE DELETION;

EID: 68549126715     PISSN: 0006291X     EISSN: 10902104     Source Type: Journal    
DOI: 10.1016/j.bbrc.2009.07.084     Document Type: Article

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