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Article

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

Neurology - 1 Apr 1998

Bennett P, Nicholl D J

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Identifiers

PMID: 9566424
DOI: 10.1212/wnl.50.4.1183

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Absence of the G209A mutation in the alpha-synuclein gene in British families with Parkinson's disease.PMID 9566424Read ↗

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

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

Novel A18T and pA29S substitutions in α-synuclein may be associated with sporadic Parkinson's diseaseSemantic proximity Read ↗

AlaSOPro mutation in the gene encoding α-synuclein in Parkinson's diseaseSemantic proximity Read ↗

Absence of SNCA polymorphisms in Pakistani Parkinsons disease patients.Semantic proximity Read ↗

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

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

The G209A mutation in the alpha-synuclein gene in Brazilian families with Parkinson's disease.Semantic proximity Read ↗

Young-onset parkinsonism due to homozygous duplication of α-synuclein in a consanguineous family.Semantic proximity Read ↗

Alpha‐synuclein and Parkinson's disease: Implications from the screening of more than 1,900 patientsSemantic 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 ↗

Cerebellar alpha-synuclein levels are decreased in Parkinson's disease and do not correlate with SNCA polymorphisms associated with disease in a Swedish material.Semantic proximity Read ↗

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