Cu/Zn superoxide dismutase (SOD1) mutations and sporadic amyotrophic lateral sclerosis
- 23 October 1993
- journal article
- other
- Published by Elsevier in The Lancet
- Vol. 342 (8878) , 1050-1051
- https://doi.org/10.1016/0140-6736(93)92905-9
Abstract
No abstract availableKeywords
This publication has 5 references indexed in Scilit:
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- Absence of linkage between chromosome 21 loci and familial amyotrophic lateral sclerosis.Journal of Medical Genetics, 1993
- Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosisNature, 1993
- The Scottish Motor Neuron Disease Register: a prospective study of adult onset motor neuron disease in Scotland. Methodology, demography and clinical features of incident cases in 1989.Journal of Neurology, Neurosurgery & Psychiatry, 1992
- Linkage of a Gene Causing Familial Amyotrophic Lateral Sclerosis to Chromosome 21 and Evidence of Genetic-Locus HeterogeneityNew England Journal of Medicine, 1991