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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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| Vydáno v: | Clin Ophthalmol |
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| Hlavní autoři: | , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Dove Medical Press
2016
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| Témata: | |
| On-line přístup: | 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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