Identification of genome-wide copy number variations and a family-based association study of avellino corneal dystrophy

Ophthalmology

Volumn 117, Issue 7, 2010, Pages

  Bae, Joon Seol ^a   Cheong, Hyun Sub ^b   Chun, Ji Yong ^a   Park, Tae Joon ^a   Kim, Ji On ^b   Kim, Eun Mi ^b   Park, Miey ^c   Kim, Dong Joon ^c   Lee, Eun Ju ^c   Kim, Eung Kweon ^d   Lee, Jong Young ^c   Shin, Hyoung Doo ^a,b  

^a Sogang University   (South Korea)

^b SNP Genetics Inc   (South Korea)

^c Korea National Institute of Health   (South Korea)

^d Yonsei University College of Medicine   (South Korea)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; AGED; ARTICLE; AVELLINO CORNEAL DYSTROPHY; CHILD; CONTROLLED STUDY; COPY NUMBER VARIATION; CORNEA DYSTROPHY; FAMILY HISTORY; FEMALE; GENE FREQUENCY; GENE MAPPING; GENOTYPE; HUMAN; KARYOTYPE; KOREA; MAJOR CLINICAL STUDY; MALE; NUCLEOTIDE SEQUENCE; PRESCHOOL CHILD; PRIORITY JOURNAL; SCHOOL CHILD;

EID: 77954348829     PISSN: 01616420     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ophtha.2009.11.021     Document Type: Article

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