Association ofLOXL1Common Sequence Variants in German and Italian Patients with Pseudoexfoliation Syndrome and Pseudoexfoliation Glaucoma
Investigative Ophthalmology & Visual Science2008Vol. 49(4), pp. 1459–1459
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Francesca Pasutto, Mandy Krumbiegel, Christian Y. Mardin, Daniela Paoli, Robert La ̈mmer, Bernhard H. F. Weber, Friedrich E. Kruse, Ursula Schlo ̈tzer-Schrehardt, André Reis
Abstract
Genetic variants in LOXL1 confer risk to PEX in German and Italian populations, independent of the presence of secondary glaucoma, confirming findings in patients from Northern Europe.
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