A founder effect and mutational hot spots may contribute to the most frequent mutations in the SPG3A gene

被引：11

作者：

Namekawa, M

Nelson, I

Ribai, P

Dürr, A

Denis, E

Stevanin, G

Ruberg, M

Brice, A

机构：

[1] Hop La Pitie Salpetriere, INSERM, U679, IFR70, F-75651 Paris 13, France

[2] Grp Hosp Pitie Salpetriere, AP HP, Dept Genet Cytogenet & Embryol, F-75634 Paris, France

[3] Grp Hosp Pitie Salpetriere, AP HP, Federat Neurol, F-75634 Paris, France

[4] Univ Paris 06, Salpetriere Med Sch, Paris, France

来源：

NEUROGENETICS | 2006年 / 7卷 / 02期

关键词：

D O I：

10.1007/s10048-006-0028-2

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

引用

页码：131 / 132

页数：2

共 5 条

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[5] SPG3A is the most frequent cause of hereditary spastic paraplegia with onset before age 10 years [J].

Namekawa, M ;

Ribai, P ;

Nelson, I ;

Forlani, S ;

Fellmann, F ;

Goizet, C ;

Depienne, C ;

Stevanin, G ;

Ruberg, M ;

Dürr, A ;

Brice, A .

NEUROLOGY, 2006, 66 (01) :112-114

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