Neuroferritinopathy in a French family with late onset dominant dystonia -: art. no. e69

被引：45

作者：

Chinnery, PF

Curtis, ARJ

Fey, C

Coulthard, A

Crompton, D

Curtis, A

Lombès, A

Burn, J

机构：

[1] Univ Newcastle Upon Tyne, Dept Neurol, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England

[2] Univ Newcastle Upon Tyne, Inst Human Genet, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England

[3] Newcastle Upon Tyne Hosp NHS Trust, Dept Radiol, Newcastle Upon Tyne, Tyne & Wear, England

[4] Hop La Pitie Salpetriere, INSERM, UR523, Inst Myol, Paris, France

来源：

JOURNAL OF MEDICAL GENETICS | 2003年 / 40卷 / 05期

关键词：

D O I：

10.1136/jmg.40.5.e69

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

[No abstract available]

引用

页数：3

共 5 条

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[4] Aconitase and mitochondrial iron-sulphur protein deficiency in Friedreich ataxia [J].

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[5] Palatal tremor and cognitive decline in neuroferritinopathy [J].

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JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2002, 73 (01) :91-92

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