Lack of association of the M129V polymorphism of the PRNP gene with pseudoexfoliation syndrome

PURPOSE: In this study we aimed to evaluate the polymorphism at codon 129 (M129V) of the PRNP gene as a secondary risk factor for pseudoexfoliation syndrome (PEX). METHODS: Two hundred and seventy-five unrelated subjects, including 156 patients with PEX and 119 unrelated control subjects, were recru...

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Publicado en:Clin Ophthalmol
Autores principales: Giannakopoulos, Marios P, Antonacopoulou, Anna G, Kottorou, Anastasia E, Kalofonos, Haralabos P, Gartaganis, Sotirios P
Formato: Artigo
Lenguaje:Inglês
Publicado: Dove Medical Press 2016
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Original Research
Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC4853150/
https://ncbi.nlm.nih.gov/pubmed/27217717
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/OPTH.S92174
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