Clinical and molecular features of patients with amyotrophic lateral sclerosis and SOD1 mutations: a monocentric study

was the first gene associated with both familial and sporadic forms of amyotrophic lateral sclerosis (ALS) and is the second most mutated gene in Caucasian ALS patients. Given their high clinical and molecular heterogeneity, a detailed characterization of -ALS patients could improve knowledge about...

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Vydáno v:	Frontiers in neurology Ročník 14; s. 1169689
Hlavní autoři:	Gagliardi, Delia, Ripellino, Paolo, Meneri, Megi, Del Bo, Roberto, Antognozzi, Sara, Comi, Giacomo Pietro, Gobbi, Claudio, Ratti, Antonia, Ticozzi, Nicola, Silani, Vincenzo, Ronchi, Dario, Corti, Stefania
Médium:	Journal Article
Jazyk:	angličtina
Vydáno:	Switzerland Frontiers Media S.A 17.05.2023
Témata:	amyotrophic lateral sclerosis cohort Neurology SOD1 variants SOD1-ALS superoxide dismutase cohort SOD1 variants SOD1-ALS amyotrophic lateral sclerosis superoxide dismutase
ISSN:	1664-2295, 1664-2295
On-line přístup:	Získat plný text
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