A loss-of-function CACNA1A mutation causing benign paroxysmal torticollis of infancy

被引：0
作者：
M Vila-Pueyo
C Sintas
M Flotats
G Gené
X Elorza
JM Fernández-Fernández
B Cormand
A Macaya
机构：
[1] Universitat Autònoma de Barcelona,Pediatric Neurology Research Group, Vall d’Hebron Research Institute
[2] University of Barcelona,Departament of Genetics, Faculty of Biology
[3] Vall d’Hebron Hospital,Pediatric Neurology Service
[4] Universitat Pompeu Fabra,Laboratory of Molecular Physiology and Channelopathies, Department of Experimental and Health Sciences
来源：
The Journal of Headache and Pain | 2013年 / 14卷
关键词：
Migraine; Migraine Attack; Head Tilt; Mutant Channel; Episodic Ataxia;
D O I：
暂无
中图分类号：
学科分类号：
摘要：
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Cuenca-Leon E(2008)Genetic analysis of 27 Spanish patients with hemiplegic migraine, basilar-type migraine and childhood periodic syndromes Cephalalgia 28 1039-47
[2]  
Corominas R(2006)CACNA1A mutation in a EA-2 patient responsive to acetazolamide and valproic acid Can J Neurol Sci 33 68-72
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