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Ubiquilin 2 mutations in Italian patients with amyotrophic lateral sclerosis and frontotemporal dementia
ALS/FTD phenotype in two Sardinian families carrying both C9ORF72 and TARDBP mutations
Infrequent SCN9A mutations in congenital insensitivity to pain and erythromelalgia
Autosomal recessive cerebellar ataxias: the current state of affairs
Pathophysiological insights into ALS with C9ORF72 expansions
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