Familial amyotrophic lateral sclerosis/motor neurone disease (FALS): a review of current developments.
Open Access
- 1 November 1995
- journal article
- review article
- Published by BMJ in Journal of Medical Genetics
- Vol. 32 (11) , 841-847
- https://doi.org/10.1136/jmg.32.11.841
Abstract
No abstract availableThis publication has 55 references indexed in Scilit:
- Superoxide dismutase and ALSThe Lancet, 1994
- A New Variant Cu/Zn Superoxide Dismutase (Val7→Glu) Deduced from Lymphocyte mRNA Sequences from Japanese Patients with Familial Amyotrophic Lateral SclerosisBiochemical and Biophysical Research Communications, 1994
- Variants of the heavy neurofilament subunit are associated with the development of amyotrophic lateral sclerosisHuman Molecular Genetics, 1994
- Analysis of the functional effects of a mutation in SOD1 associated with familial amyotrophic lateral sclerosisNeuron, 1994
- A Novel Mutation in Cu/Zn Superoxide Dismutase Gene in Japanese Familial Amyotrophic Lateral SclerosisBiochemical and Biophysical Research Communications, 1994
- The Cu/Zn superoxide dismutase gene in ALS and Parkinsonism-dementia of GuamNeuroReport, 1994
- Progressive neuronopathy in transgenic mice expressing the human neurofilament heavy gene: A mouse model of amyotrophic lateral sclerosisCell, 1993
- 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
- Phenotypic and genotypic heterogeneity of dominantly inherited amyotrophic lateral sclerosisActa Neurologica Scandinavica, 1987