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Analysis of STMN2 CA repeats in italian ALS patients shows no association.

Amyotrophic lateral sclerosis & frontotemporal degeneration - 1 Feb 2023

Doronzio Paolo Niccolò, Lattante Serena, Marangi Giuseppe, Martello Francesco, Conte Amelia, Bisogni Giulia, Bernardo Daniela, Patanella Agata Katia, Meleo Emiliana, Zollino Marcella, Sabatelli Mario

Abstract excerpt

Amyotrophic Lateral Sclerosis (ALS) is a fatal neurodegenerative disease caused by a complex interaction of genetic and environmental factors. Recently, a polymorphic intronic CA repeat in STMN2 gene has been proposed as risk factor for ALS. The presence of long/long CA genotype, especially if one allele had 24 CA, was reported to be significantly associated with the disease in a cohort of sporadic ALS patients....

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PMID: 35876065
DOI: 10.1080/21678421.2022.2102430

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