Associated Papers
Novel in-frame duplication variant of SOD1 in a Japanese family with familial amyotrophic lateral sclerosis.
Nakajima M et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration, 2025
Infantile SOD1 deficiency syndrome caused by a homozygous SOD1 variant with absence of enzyme activity.
Ezer S et al.
Brain : a Journal of Neurology, 2022
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