Spinocerebellar ataxia type 10 is rare in populations other than Mexicans

被引：37

作者：

Matsuura, T

Ranum, LPW

Volpini, V

Pandolfo, M

Sasaki, H

Tashiro, K

Watase, K

Zoghbi, HY

Ashizawa, T ^{[1
]}

机构：

[1] Baylor Coll Med, Dept Neurol, Houston, TX 77030 USA

[2] Baylor Coll Med, Dept Mol & Human Genet, Houston, TX 77030 USA

[3] Vet Affairs Med Ctr, Houston, TX USA

[4] Univ Minnesota, Dept Genet, Minneapolis, MN 55455 USA

[5] Univ Minnesota, Dept Cell & Dev Biol, Minneapolis, MN 55455 USA

[6] Univ Minnesota, Inst Human Genet, Minneapolis, MN 55455 USA

[7] Duran I Reynals Hosp, IRO, Med & Mol Genet Ctr, Barcelona, Spain

[8] Ctr Hosp Univ Montreal, Quebec City, PQ, Canada

[9] Hokkaido Univ, Sch Med, Dept Neurol, Sapporo, Hokkaido 060, Japan

来源：

NEUROLOGY | 2002年 / 58卷 / 06期

关键词：

D O I：

10.1212/WNL.58.6.983

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

引用

页码：983 / 984

页数：2

共 6 条

[1] Clinical and genetic analysis of a distinct autosomal dominant spinocerebellar ataxia [J].

Grewal, RP ;

Tayag, E ;

Figueroa, KP ;

Zu, L ;

Durazo, A ;

Nunez, C ;

Pulst, SM .

NEUROLOGY, 1998, 51 (05) :1423-1426

[2] Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10 [J].

Matsuura, T ;

Yamagata, T ;

Burgess', DL ;

Rasmussen, A ;

Grewal, RP ;

Watase, K ;

Khajavi, M ;

McCall, AE ;

Davis, CF ;

Zu, L ;

Achari, M ;

Pulst, SM ;

Alonso, E ;

Noebels, JL ;

Nelson, DL ;

Zoghbi, HY ;

Ashizawa, T .

NATURE GENETICS, 2000, 26 (02) :191-194

[3]

Matsuura T, 1999, ANN NEUROL, V45, P407, DOI 10.1002/1531-8249(199903)45:3<407::AID-ANA21>3.0.CO

[4]

2-D

[5]

Rasmussen A, 2000, AM J HUM GENET, V67, P342

[6] Mapping of a new autosomal dominant spinocerebellar ataxia to chromosome 22 [J].

Zu, L ;

Figueroa, KP ;

Grewal, R ;

Pulst, SM .

AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 64 (02) :594-599

← 1 →