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).

Common sequence variants in the LOXL1 gene in pigment dispersion syndrome and pigmentary glaucoma / Giardina, Emiliano; Oddone, F; Lepre, T; Centofanti, Marco; Peconi, C; Tanga, L; Quaranta, L; Frezzotti, P; Novelli, Giuseppe; Manni, Gianluca. - In: BMC OPHTHALMOLOGY. - ISSN 1471-2415. - 14:1(2014), pp. 52-52. [10.1186/1471-2415-14-52]

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

MANNI, GIANLUCA
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).
2014
01 Pubblicazione su rivista::01a Articolo in rivista
Common sequence variants in the LOXL1 gene in pigment dispersion syndrome and pigmentary glaucoma / Giardina, Emiliano; Oddone, F; Lepre, T; Centofanti, Marco; Peconi, C; Tanga, L; Quaranta, L; Frezzotti, P; Novelli, Giuseppe; Manni, Gianluca. - In: BMC OPHTHALMOLOGY. - ISSN 1471-2415. - 14:1(2014), pp. 52-52. [10.1186/1471-2415-14-52]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/1738370
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