A novel central motor conduction abnormality in D90A-homozygous patients with amyotrophic lateral sclerosis.

Patients with amyotrophic lateral sclerosis (ALS) who are homozygous for the D90A SOD1 mutation have been noted to have central motor abnormalities distinct from those of patients with idiopathic ALS. We stimulated the motor cortex of ten patients homozygous for the D90A SOD1 mutation, using transcr...

ver descrição completa

Detalhes bibliográficos
Main Authors: Osei-Lah, A, Turner, M, Andersen, P, Leigh, P, Mills, K
Formato: Journal article
Idioma:English
Publicado em: 2004

Registos relacionados