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).

Giardina, E., Oddone, F., Lepre, T., Centofanti, M., Peconi, C., Tanga, L., et al. (2014). Common sequence variants in the LOXL1 gene in pigment dispersion syndrome and pigmentary glaucoma. BMC OPHTHALMOLOGY, 14(1), 52-52 [10.1186/1471-2415-14-52].

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

GIARDINA, EMILIANO;CENTOFANTI, MARCO;NOVELLI, GIUSEPPE;MANNI, GIANLUCA
2014-01-01

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
Pubblicato
Rilevanza internazionale
Articolo
Sì, ma tipo non specificato
Settore MED/03 - GENETICA MEDICA
English
Giardina, E., Oddone, F., Lepre, T., Centofanti, M., Peconi, C., Tanga, L., et al. (2014). Common sequence variants in the LOXL1 gene in pigment dispersion syndrome and pigmentary glaucoma. BMC OPHTHALMOLOGY, 14(1), 52-52 [10.1186/1471-2415-14-52].
Giardina, E; Oddone, F; Lepre, T; Centofanti, M; Peconi, C; Tanga, L; Quaranta, L; Frezzotti, P; Novelli, G; Manni, G
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/85896
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