Autosomal-dominant proximal spinal muscular atrophy caused by mutations in a novel gene-motor adaptor BICD2

被引：0
|
作者：
Peeters, K. [1 ,2 ]
Litvinenko, I. [3 ]
Chamova, T. [4 ]
Asselbergh, B. [2 ,5 ]
Almeida-Souza, L. [2 ,6 ]
Geuens, T. [2 ,6 ]
Ydens, E. [2 ,6 ]
Zimon, M. [1 ,2 ]
Irobi, J. [5 ]
De Vriendt, E. [1 ,2 ]
De Winter, V. [2 ,6 ]
Ooms, T. [1 ,2 ]
Timmerman, V. [2 ,6 ]
Tournev, I. [4 ,7 ]
Jordanova, A. [1 ,2 ,8 ]
机构：
[1] Univ Antwerp VIB, Mol Neurogen Grp, Dept Mol Genet, B-2610 Antwerp, Belgium
[2] Univ Antwerp, Inst Born Bunge, Neurogenet Lab, B-2020 Antwerp, Belgium
[3] Med Univ, Clin Child Neurol, Dept Pediat, Sofia, Bulgaria
[4] Med Univ, Dept Neurol, Univ Hosp Alexandrovska, Fac Med, Sofia, Bulgaria
[5] Univ Antwerp VIB, Dept Mol Genet, Cent Serv Fac, B-2610 Antwerp, Belgium
[6] Univ Antwerp VIB, Dept Mol Genet, Peripheral Neuropathy Grp, B-2610 Antwerp, Belgium
[7] New Bulgarian Univ, Dept Cognit Sci & Psychol, Sofia, Bulgaria
[8] Med Univ, Mol Med Ctr, Dept Med Chem & Biochem, Sofia, Bulgaria
来源：
JOURNAL OF NEUROLOGY | 2014年 / 261卷
关键词：
D O I：
暂无
中图分类号：
R74 [神经病学与精神病学];
学科分类号：
摘要：
OS3219
引用
收藏
页码：S67 / S68
页数：2
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