Ion channels and neurology.
作者信息
Zuberi S M, Hanna M G
机构信息
Fraser of Allander Neurosciences Unit, Royal Hospital for Sick Children, Yorkhill, Glasgow G3 8SJ, UK.
出版信息
Arch Dis Child. 2001 Mar;84(3):277-80. doi: 10.1136/adc.84.3.277.
Abstract
摘要
相似文献
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Arch Dis Child. 2001 Mar;84(3):277-80. doi: 10.1136/adc.84.3.277.
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CHRNB2 is the second acetylcholine receptor subunit associated with autosomal dominant nocturnal frontal lobe epilepsy.CHRNB2是与常染色体显性遗传性夜间额叶癫痫相关的第二个乙酰胆碱受体亚基。
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Ion channels and epilepsy in man and mouse.人类和小鼠中的离子通道与癫痫
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Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2.两个患有GEFS+2的家族中编码神经元钠通道的SCN1A发生突变。
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A novel mutation in the human voltage-gated potassium channel gene (Kv1.1) associates with episodic ataxia type 1 and sometimes with partial epilepsy.人类电压门控钾通道基因（Kv1.1）中的一种新突变与1型发作性共济失调相关，有时也与部分性癫痫相关。
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Generalized epilepsy with febrile seizures plus: a common childhood-onset genetic epilepsy syndrome.伴有热性惊厥附加症的全身性癫痫：一种常见的儿童期起病的遗传性癫痫综合征。
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KCNQ2 and KCNQ3 potassium channel subunits: molecular correlates of the M-channel.KCNQ2和KCNQ3钾通道亚基：M通道的分子关联
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10
Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel beta1 subunit gene SCN1B.热性惊厥和与钠离子通道β1亚基基因SCN1B突变相关的全身性癫痫。
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