Clinical and Neuropathological Features of Spastic Ataxia in a Spanish Family with Novel Compound Heterozygous Mutations in STUB1

被引:32
|
作者
Bettencourt, Conceicao [1 ,2 ,3 ,4 ]
Garcia de Yebenes, Justo [5 ]
Luis Lopez-Sendon, Jose [5 ]
Shomroni, Orr [6 ]
Zhang, Xingqian [7 ]
Qian, Shu-Bing [7 ]
Bakker, Ingrid M. C. [6 ]
Heetveld, Sasja [6 ]
Ros, Raquel [5 ]
Quintans, Beatriz [8 ,9 ]
Sobrido, Maria-Jesus [8 ,9 ]
Bevova, Marianna R. [6 ,10 ]
Jain, Shushant [6 ,11 ]
Bugiani, Marianna [12 ,13 ]
Heutink, Peter [6 ,11 ]
Rizzu, Patrizia [6 ,11 ]
机构
[1] UCL Inst Neurol, Dept Mol Neurosci, London, England
[2] Univ Porto, Inst Mol & Cell Biol, P-4100 Oporto, Portugal
[3] Univ Azores, Ctr Res Nat Resources CIRN, Ponta Delgada, Portugal
[4] Univ Azores, Dept Biol, Ponta Delgada, Portugal
[5] Hosp Ramon & Cajal, Dept Neurol, E-28034 Madrid, Spain
[6] Vrije Univ Amsterdam Med Ctr, Dept Clin Genet, Amsterdam, Netherlands
[7] Cornell Univ, Div Nutr Sci, Ithaca, NY USA
[8] Clin Hosp Santiago de Compostela SERGAS, Fdn Publ Galega Med Xenom, Santiago De Compostela, Spain
[9] Clin Hosp Santiago de Compostela SERGAS, Hlth Res Inst Santiago de Compostela IDIS, Santiago De Compostela, Spain
[10] European Res Inst Biol Ageing, Groningen, Netherlands
[11] German Ctr Neurodegenerat Dis, Tubingen, Germany
[12] Vrije Univ Amsterdam Med Ctr, Dept Pediat, Child Neurol, Amsterdam, Netherlands
[13] Vrije Univ Amsterdam Med Ctr, Dept Pathol, Amsterdam, Netherlands
来源
CEREBELLUM | 2015年 / 14卷 / 03期
关键词
Autosomal Recessive Inheritance; Compound Heterozygous Mutation; Neuronal Intranuclear Inclusion; Ocular Pursuit; Neurogenic Dysphagia;
D O I
10.1007/s12311-014-0643-7
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
引用
收藏
页码:378 / 381
页数:4
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