PubMed · 1995 · 121 citations · 11 references
Life SciencesGeneticsMolecular GeneticsMedical GeneticsNeurodegenerationNeurogeneticsAmyotrophic Lateral SclerosisMolecular NeurogeneticsMotor Neuron DiseasesNeurodegenerative Disease GeneticsNeurodegenerative DiseasesNeurodegenerative DisordersAmyotrophic Lateral Sclerosis PathologyFamilial Neurodegenerative DiseaseHereditary Motor Neuron DiseaseNeurodegeneration GeneticsNeurodegenerative GeneticsSod1 PathologySuperoxide Dismutase Function
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disorder affecting motor neurons. Although most cases of ALS are sporadic, approximately 10% are inherited as an autosomal dominant trait. Mutations in the Cu/Zn superoxide dismutase gene (SOD 1) are responsible for a fraction of familial ALS (FALS). Screening our FALS kindreds by SSCP, we have identified mutations in 15 families, of which 9 have not been previously reported. Two of the new mutations alter amino acids that have never been implicated in FALS. One of them affects a highly conserved amino acid involved in dimer contact, and the other one affects the active-site loop of the enzyme. These two mutations reduce significantly SOD 1 enzyme activity in lymphoblasts. Our results suggest that SOD 1 mutations are responsible for > or = 13% of FALS cases.
11
Primer-Directed Enzymatic Amplification of DNA with a Thermostable DNA Polymerase
Randall K. Saiki, David H. Gelfand, Susanne Stoffel et al. · Science · 1988 · 17.2K citations