A novel mutation producing premature termination codon at the OPA1 gene causes autosomal dominant optic atrophy

被引：0

作者：

E. Cardaioli

G. N. Gallus

P. Da Pozzo

A. Rufa

R. Franceschini

E. Motolese

A. Caporossi

M. T. Dotti

A. Federico

机构：

[1] Medical School,Department of Neurological and Behavioural Sciences

[2] University of Siena,Department of Ophthalmological and Neurosurgical Sciences

[3] University of Siena,undefined

来源：

Journal of Neurology | 2006年 / 253卷

关键词：

Optic Neuropathy; Optic Atrophy; Premature Termination Codon; Autosomal Dominant Optic Atrophy; OPA1 Gene;

D O I：

暂无

中图分类号：

学科分类号：

摘要：

引用

页码：672 / 673

页数：1

共 11 条

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