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pubmed-article:20202685pubmed:abstractTextTo determine the association of identified copy number variations (CNVs) in whole genome with the risk of Avellino corneal dystrophy (ACD) in a Korean population.lld:pubmed
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pubmed-article:20202685pubmed:copyrightInfoCopyright 2010 American Academy of Ophthalmology. Published by Elsevier Inc. All rights reserved.lld:pubmed
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pubmed-article:20202685pubmed:articleTitleIdentification of genome-wide copy number variations and a family-based association study of Avellino corneal dystrophy.lld:pubmed
pubmed-article:20202685pubmed:affiliationLaboratory of Genomic Diversity, Department of Life Science, Sogang University, Shinsu-dong, Mapo-gu, Seoul, Republic of Korea.lld:pubmed
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