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pmid: 14593171
Mutations in the α-synuclein gene ( SNCA ) in the Contursi kindred ([ 1 ][1]) implicated this gene in Parkinson's disease (PD). Subsequently, α-synuclein was identified as the major component of Lewy bodies, the pathological hallmark of PD, and of glial cell cytoplasmic inclusions ([ 2 ][2]). We
Male, Genetic Linkage, Reverse Transcriptase Polymerase Chain Reaction, Gene Dosage, Synucleins, Nerve Tissue Proteins, Parkinson Disease, Exons, Polymorphism, Single Nucleotide, Pedigree, Haplotypes, Mutation, alpha-Synuclein, Humans, Family, Female, Promoter Regions, Genetic, Alleles, In Situ Hybridization, Fluorescence
Male, Genetic Linkage, Reverse Transcriptase Polymerase Chain Reaction, Gene Dosage, Synucleins, Nerve Tissue Proteins, Parkinson Disease, Exons, Polymorphism, Single Nucleotide, Pedigree, Haplotypes, Mutation, alpha-Synuclein, Humans, Family, Female, Promoter Regions, Genetic, Alleles, In Situ Hybridization, Fluorescence
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