Maintaining the balance: both gain- and loss-of-function KCNA2 mutants cause epileptic encephalopathy

被引:3
作者
Droegemoeller, B. I. [1 ]
机构
[1] Univ British Columbia, Canadian Pharmacogen Network Drug Safety, Dept Pediat, Vancouver, BC V5Z 1M9, Canada
基金
英国惠康基金;
关键词
MUTATIONS;
D O I
10.1111/cge.12615
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathy Syrbe et al. (2015) Nat Genet 47(4):393-99
引用
收藏
页码:137 / 139
页数:3
相关论文
共 3 条
[1]   De novo mutations in epileptic encephalopathies [J].
Allen, Andrew S. ;
Berkovic, Samuel F. ;
Cossette, Patrick ;
Delanty, Norman ;
Dlugos, Dennis ;
Eichler, Evan E. ;
Epstein, Michael P. ;
Glauser, Tracy ;
Goldstein, David B. ;
Han, Yujun ;
Heinzen, Erin L. ;
Hitomi, Yuki ;
Howell, Katherine B. ;
Johnson, Michael R. ;
Kuzniecky, Ruben ;
Lowenstein, Daniel H. ;
Lu, Yi-Fan ;
Madou, Maura R. Z. ;
Marson, Anthony G. ;
Mefford, Heather C. ;
Nieh, Sahar Esmaeeli ;
O'Brien, Terence J. ;
Ottman, Ruth ;
Petrovski, Slave ;
Poduri, Annapurna ;
Ruzzo, Elizabeth K. ;
Scheffer, Ingrid E. ;
Sherr, Elliott H. ;
Yuskaitis, Christopher J. ;
Abou-Khalil, Bassel ;
Alldredge, Brian K. ;
Bautista, Jocelyn F. ;
Berkovic, Samuel F. ;
Boro, Alex ;
Cascino, Gregory D. ;
Consalvo, Damian ;
Crumrine, Patricia ;
Devinsky, Orrin ;
Dlugos, Dennis ;
Epstein, Michael P. ;
Fiol, Miguel ;
Fountain, Nathan B. ;
French, Jacqueline ;
Friedman, Daniel ;
Geller, Eric B. ;
Glauser, Tracy ;
Glynn, Simon ;
Haut, Sheryl R. ;
Hayward, Jean ;
Helmers, Sandra L. .
NATURE, 2013, 501 (7466) :217-+
[2]   Dominant-negative effects of KCNQ2 mutations are associated with epileptic encephalopathy [J].
Orhan, Goekce ;
Bock, Merle ;
Schepers, Dorien ;
Ilina, Elena I. ;
Reichel, Stephanie Nadine ;
Loeffler, Heidi ;
Jezutkovic, Nicole ;
Weckhuysen, Sarah ;
Mandelstam, Simone ;
Suls, Arvid ;
Danker, Timm ;
Guenther, Elke ;
Scheffer, Ingrid E. ;
De Jonghe, Peter ;
Lerche, Holger ;
Maljevic, Snezana .
ANNALS OF NEUROLOGY, 2014, 75 (03) :382-394
[3]   Ataxia and myoclonic epilepsy due to a heterozygous new mutation in KCNA2: proposal for a new channelopathy [J].
Pena, S. D. J. ;
Coimbra, R. L. M. .
CLINICAL GENETICS, 2015, 87 (02) :E1-E3