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Genome-wide association study with DNA pooling identifies variants at CNTNAP2 associated with pseudoexfoliation syndrome

Krumbiegel, M, Pasutto, F, Schlötzer-Schrehardt, U, Uebe, S, Zenkel, M, Mardin, C Y, Weisschuh, N, Paoli, D, Gramer, E, Becker, C, Ekici, A B, Weber, Bernhard H. F. , Nürnberg, P, Kruse, F E and Reis, A (2011) Genome-wide association study with DNA pooling identifies variants at CNTNAP2 associated with pseudoexfoliation syndrome. European Journal of Human Genetics 19 (2), pp. 186-193.

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Abstract

Genetic and nongenetic factors contribute to development of pseudoexfoliation (PEX) syndrome, a complex, age-related, generalized matrix process frequently associated with glaucoma. To identify specific genetic variants underlying its etiology, we performed a genome-wide association study (GWAS) using a DNA-pooling approach. Therefore, equimolar amounts of DNA samples of 80 subjects with PEX ...

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Item type:Article
Date:2011
Institutions:Medicine > Lehrstuhl für Humangenetik
Identification Number:
ValueType
10.1038/ejhg.2010.144DOI
20808326PubMed ID
Keywords:pseudoexfoliation syndrome; DNA pooling; association study
Dewey Decimal Classification:600 Technology > 610 Medical sciences Medicine
Status:Published
Refereed:Yes, this version has been refereed
Created at the University of Regensburg:Partially
Item ID:35490
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