Genetic inroads in familial ALS.

This publication has 13 references indexed in Scilit:

• The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis
  Nature Genetics, 2001
• A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2
  Nature Genetics, 2001
• Homozygous deletion of the survival motor neuron 2 gene is a prognostic factor in sporadic ALS
  Neurology, 2001
• Oxidation versus aggregation — how do SOD1 mutants cause ALS?
  Nature Medicine, 2000
• Analysis of chromosome 5q13 genes in amyotrophic lateral sclerosis: Homozygous naip deletion in a sporadic case
  Annals of Neurology, 1996
• Association of apolipoprotein E ∈4 allele with bulbar-onset motor neuron disease
  The Lancet, 1996
• Variants of the heavy neurofilament subunit are associated with the development of amyotrophic lateral sclerosis
  Human Molecular Genetics, 1994
• Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33–q35
  Nature Genetics, 1994
• Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis
  Nature, 1993
• HEREDITARY MOTOR SYSTEM DISEASES (CHRONIC JUVENILE AMYOTROPHIC LATERAL SCLEROSIS)
  Brain, 1990