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Familial amyotrophic lateral sclerosis with His46Arg mutation in Cu/Zn superoxide dismutase presenting characteristic clinical features and Lewy body-like hyaline inclusions

Amyotrophic Lateral SclerosisMendelian DisorderNeurological DisorderPathologyNeurologyNeuroscienceNeurodegenerationHis46arg MutationNeuropathologyMedicineCu/zn Superoxide DismutaseCharacteristic Clinical Features