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

INTRODUCTION: SOD1 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 SOD1-ALS patients could i...

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Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10230028/
https://www.ncbi.nlm.nih.gov/pubmed/37265463
http://dx.doi.org/10.3389/fneur.2023.1169689

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10230028/
https://www.ncbi.nlm.nih.gov/pubmed/37265463
http://dx.doi.org/10.3389/fneur.2023.1169689

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