Spinocerebellar ataxia with mental retardation (SCA13)

被引：0

作者：

Giovanni Stevanin

Alexandra Durr

Nawal Benammar

Alexis Brice

机构：

[1] INSERM U679 (former U289),Department of Genetics Cytogenetics and Embryology

[2] Hôpital de la Salpêtrière,Federation of Neurology

[3] 47,undefined

[4] Boulevard de l’Hôpital,undefined

[5] AP-HP,undefined

[6] Salpetriere hospital,undefined

[7] AP-HP,undefined

[8] Salpetriere hospital,undefined

[9] Pitie-Salpetriere Medical School,undefined

[10] Pierre and Marie Curie University,undefined

来源：

The Cerebellum | 2005年 / 4卷

关键词：

Spinocerebellar ataxias; spinocerebellar degenerations; mental retardation; linkage (genetics); chromosome mapping;

D O I：

暂无

中图分类号：

学科分类号：

摘要：

Spinocerebellar ataxia 13 is a slowly progressive and relatively pure autosomal dominant cerebellar ataxia with childhood onset and mental deficiency. The responsible gene has been assigned to a 5.2 Mbases interval on chromosome 19q in a single French family.

引用

页码：43 / 46

页数：3

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