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, 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.
Fulltext not available.
Krumbiegel, M., Pasutto, F., Mardin, C. Y., Weisschuh, N., Paoli, D., Gramer, E., Zenkel, M., Weber, Bernhard H. F.
, Kruse, F. E., Schlötzer-Schrehardt, U. and Reis, A.
(2009)
Exploring functional candidate genes for genetic association in German patients with pseudoexfoliation syndrome and pseudoexfoliation glaucoma.
Investigative ophthalmology and visual science 50 (6), pp. 2796-2801.
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