Homozygous deletions in parkin gene in European and North African families with autosomal recessive juvenile parkinsonism

被引：169

作者：

Lücking, CB

Abbas, N

Dürr, A

Bonifati, V

Bonnet, AM

de Broucker, T

De Michele, G

Wood, NW

Agid, Y

Brice, A ^{[1
]}

机构：

[1] Hop La Pitie Salpetriere, INSERM, U289, F-75651 Paris 13, France

[2] Univ La Sapienza, Dipartimento Sci Neurol, Rome, Italy

[3] Hop Casanova, Serv Neurol, St Denis, France

[4] Univ Naples Federico II, Dipartimento Sci Neurol, Naples, Italy

[5] Inst Neurol, London WC1N 3BG, England

来源：

LANCET | 1998年 / 352卷 / 9137期

关键词：

D O I：

10.1016/S0140-6736(05)60746-5

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

[No abstract available]

引用

页码：1355 / 1356

页数：2

共 5 条

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[5] Chromosome 6-linked autosomal recessive early-onset parkinsonism:: Linkage in European and Algerian families, extension of the clinical spectrum, and evidence of a small homozygous deletion in one family [J].

Tassin, J ;

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Abbas, N ;

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