Pitfalls in ataxia with ocular motor apraxia type 1: pseudodominant inheritance and very late onset

被引：0

作者：

Chloé Laurencin

Mathieu Anheim

Lise Larrieu

Caroline Tilikete

Michel Koenig

Stéphane Thobois

机构：

[1] Hospices Civils de Lyon,Neurologie C

[2] Hôpital Neurologique Pierre Wertheimer,Faculté de Médecine Lyon Sud Charles Mérieux

[3] Université de Lyon,Institut de Génétique et de Biologie Moléculaire et Cellulaire, CNRS, INSERM

[4] Université Lyon 1,Département de Neurologie

[5] CNRS,Laboratoire de Génétique des Maladies Rares

[6] Centre de Neurosciences Cognitives,Neurologie D

[7] UMR 5229,Lyon Neuroscience Research Center

[8] Université de Strasbourg,undefined

[9] Hospices Civils de Strasbourg,undefined

[10] Institut Universitaire de Recherche Clinique,undefined

[11] Hospices Civils de Lyon,undefined

[12] Hôpital Neurologique Pierre Wertheimer,undefined

[13] INSERM U1028,undefined

[14] IMPACT Team,undefined

来源：

Journal of Neurology | 2015年 / 262卷

关键词：

Cerebellar Ataxia; Spinocerebellar Ataxia; Cerebellar Atrophy; Ataxia Telangiectasia; Axonal Neuropathy;

D O I：

暂无

中图分类号：

学科分类号：

摘要：

引用

页码：1366 / 1368

页数：2

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