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
收藏
页码：1366 / 1368
页数：2
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