PON1 is a disease modifier gene in amyotrophic lateral sclerosis: association of the Q192R polymorphism with bulbar onset and reduced survival
Articolo
Data di Pubblicazione:
2019
Abstract:
Previous studies have associated single-nucleotide polymorphisms (SNPs) in the gene encoding the detoxifying enzyme paraoxonase 1 (PON1) to the risk of sporadic ALS. Here, we aimed to assess the role of the coding rs662 (Q192R) SNP as a modifier of ALS phenotype.
Tipologia CRIS:
1.1 Articolo in rivista
Keywords:
ALS; Motor neurons; PON1; Paraoxonase; SNP; Toxicity
Elenco autori:
Verde, Federico; Tiloca, Cinzia; Morelli, Claudia; Doretti, Alberto; Poletti, Barbara; Maderna, Luca; Messina, Stefano; Gentilini, Davide; Fogh, Isabella; Ratti, Antonia; Silani, Vincenzo; Ticozzi, Nicola
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