Common sequence variants in the LOXL1 gene in pigment dispersion syndrome and pigmentary glaucoma

BACKGROUND: Single nucleotide polymorphisms (SNPs) within the LOXL1 gene are associated with pseudoesfoliation syndrome and pseudoesfoliation glaucoma. The aim of our study is to investigate a potential involvement of LOXL1 gene in the pathogenesis of pigment dispersion syndrome (PDS) and pigmentary...

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Detalhes bibliográficos
Main Authors: Giardina, Emiliano, Oddone, Francesco, Lepre, Tiziana, Centofanti, Marco, Peconi, Cristina, Tanga, Lucia, Quaranta, Luciano, Frezzotti, Paolo, Novelli, Giuseppe, Manni, Gianluca
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2014
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Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4028282/
https://ncbi.nlm.nih.gov/pubmed/24739284
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2415-14-52
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