Common sequence variants in the LOXL1 gene in pigment dispersion syndrome and pigmentary glaucoma
Articolo
Data di Pubblicazione:
2014
Abstract:
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 glaucoma (PG).
Tipologia CRIS:
1.1 Articolo in rivista
Keywords:
Amino Acid Oxidoreductases; Female; Gene Frequency; Genotype; Glaucoma, Open-Angle; Haplotypes; Humans; Intraocular Pressure; Male; Middle Aged; RNA; Real-Time Polymerase Chain Reaction; Genetic Variation
Elenco autori:
Giardina, Emiliano; Oddone, Francesco; Lepre, Tiziana; Centofanti, Tiziana; Peconi, Tiziana; Tanga, Lucia; Quaranta, Luciano; Frezzotti, Paolo; Novelli, Giuseppe; Manni, Gianluca
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