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Article

Genetic Analysis of Families with Parkinson Disease that Carry the Ala53Thr Mutation in the Gene Encoding α-Synuclein

1 Aug 1999

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 10417297
DOI: 10.1086/302486

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Related research

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Genetic Analysis of Families with Parkinson Disease that Carry the Ala53Thr Mutation in the Gene Encoding α-SynucleinPMID 10417297Read ↗

Analysis of the α-synuclein G209A mutation in familial Parkinson's diseaseSemantic proximity Read ↗

The alpha-synuclein Ala53Thr mutation is not a common cause of familial Parkinson's disease: a study of 230 European cases. European Consortium on Genetic Susceptibility in Parkinson's Disease.Semantic proximity Read ↗

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Absence of the G209A mutation in the alpha-synuclein gene in British families with Parkinson's disease.Semantic proximity Read ↗

Phenotypic spectrum of alpha-synuclein mutations: New insights from patients and cellular models.Semantic proximity Read ↗

α-synuclein locus duplication as a cause of familial Parkinson's diseaseSemantic proximity Read ↗

The genetics and molecular biology of alpha-synuclein.Semantic proximity Read ↗

Clinical and pathological features of a Parkinsonian syndrome in a family with an Ala53Thr alpha-synuclein mutation.Semantic proximity Read ↗

Mutation in the alpha-synuclein gene and sporadic Parkinson's disease, Alzheimer's disease, and dementia with lewy bodies.Semantic proximity Read ↗

Genetics of synucleins in neurodegenerative diseasesSemantic proximity Read ↗

Absence of mutation in the beta- and gamma-synuclein genes in familial autosomal dominant Parkinson's disease.Semantic proximity Read ↗

Sequencing of the alpha-synuclein gene in a large series of cases of familial Parkinson's disease fails to reveal any further mutations. The European Consortium on Genetic Susceptibility in Parkinson's Disease (GSPD)Semantic proximity Read ↗

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