6533b834fe1ef96bd129d7c4
RESEARCH PRODUCT
Further evidence that D90A-SOD1 mutation is recessively inherited in ALS patients in Italy.
Maria Rosaria MonsurròAldo QuattroneVincenzo La BellaMaria MugliaIsa Laura SimoneAngela MagarielloA. L. GabrieleCarmine UngaroLuigi CitrignoGioacchino TedeschiAlessandra PatitucciRosalucia MazzeiPaola ValentinoStefano ZoccolellaAlessandro TessitoreFrancesco BonoTeresa SprovieriG. MajoranaFrancesca Luisa Confortisubject
AdultMaleGenotypeSOD1DNA Mutational AnalysisGenes RecessiveBiologyGenetic analysisSuperoxide dismutaseSuperoxide Dismutase-1GenotypemedicineHumansGenetic Predisposition to DiseaseAmyotrophic lateral sclerosisGeneDe novo mutationsAgedGeneticsSuperoxide DismutaseAmyotrophic Lateral SclerosisSOD1; SLA;General MedicineSOD1Middle Agedmedicine.diseaseMolecular biologyNeurologyItalyMutation (genetic algorithm)Mutationbiology.proteinFemaleNeurology (clinical)SLAdescription
Mutations in the Cu/Zn superoxide dismutase 1 (SOD1) gene have been reported to cause adult-onset autosomal dominant amyotrophic lateral sclerosis (FALS). In sporadic cases (SALS), de novo mutations in the SOD1 gene have occasionally been observed. All the SOD1 mutations are autosomal dominantly inherited with the exception of D90A. To date, in Italy, only two sporadic ALS cases carrying the D90A mutation have been reported in a homozygous state. We investigated for the presence of this mutation in 169 unrelated ALS patients from southern Italy. The genetic analysis revealed three ALS patients (1.8%) with mild phenotype carrying the homozygous D90A mutation.
year | journal | country | edition | language |
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2008-01-01 |