Genetic analysis of families with Parkinson disease that carry the Ala53Thr mutation in the gene encoding α-synuclein

被引：107

作者：

Athanassiadou, A ^{[1
]}

Voutsinas, G

Psiouri, L

Leroy, E

Polymeropoulos, MH

Ilias, A

Maniatis, GM

Papapetropoulos, T

机构：

[1] Univ Patras, Fac Med, Dept Biol, Patras, Greece

[2] Univ Patras, Fac Med, Dept Neurol, Patras, Greece

[3] Natl Human Genome Res Inst, Lab Genet Dis Res, NIH, Bethesda, MD USA

[4] Novartis Pharmaceut Corp, Pharmacogenet, Gaithersburg, MD USA

[5] Univ Athens, Eginit Hosp, Athens, Greece

来源：

AMERICAN JOURNAL OF HUMAN GENETICS | 1999年 / 65卷 / 02期

关键词：

D O I：

10.1086/302486

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：555 / 558

页数：4

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[31] Lack of α-synuclein gene mutations in families with autosomal dominant Parkinson's disease in Russia [J].

Illarioshkin, SN ;

Ivanova-Smolenskaya, IA ;

Markova, ED ;

Zagorovskaya, TB ;

Brice, A .

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[32] Genetic studies in Parkinson's disease with an α-synuclein/NACP gene polymorphism in Japan [J].

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Morino, H ;

Oda, M ;

Maruyama, H ;

Udaka, F ;

Kameyama, M ;

Nakamura, S ;

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[39] A new alpha-synuclein missense variant (Thr72Met) in two Turkish families with Parkinson's disease [J].

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[40] Mutation in the α-synuclein gene and sporadic Parkinson's disease, Alzheimer's disease, and dementia with Lewy bodies [J].

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