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
收藏
页码：43 / 46
页数：3
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