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Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci.
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Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci.
Genetic association study of exfoliation syndrome identifies a protective rare variant at LOXL1 and five new susceptibility loci. Nat Genet. 2017 07; 49(7):993-1004.
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PubMed
subject areas
Aged, 80 and over
Alleles
Amino Acid Oxidoreductases
Amino Acid Substitution
Calcium Channels
Cell Adhesion
Exfoliation Syndrome
Extracellular Matrix
Eye
Female
Gene Expression Profiling
Genetic Predisposition to Disease
Genome-Wide Association Study
Haplotypes
Humans
Male
Molecular Chaperones
Mutation, Missense
Point Mutation
RNA, Messenger
Spheroids, Cellular
authors with profiles
Peter Kraft, Ph.D.
Janey Lee Wiggs, M.D., Ph.D.
Bradford John Shingleton, M.D.
Soumya Raychaudhuri, M.D., Ph.D.
Jae Hee Kang, Sc.D.