A Missense Mutation in the Sodium Channel Scn8a Is Responsible for Cerebellar Ataxia in the Mouse Mutant jolting (October, pg 5993, 1996)

被引：0

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作者：

Kohrman, David C.

Smith, Marianne R.

Goldin, Alan L.

Harris, John

Meisler, Miriam H.

机构：

来源：

JOURNAL OF NEUROSCIENCE | 2013年 / 33卷 / 11期

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D O I：

10.1523/JNEUROSCI.0722-13.2013

中图分类号：

Q189 [神经科学];

学科分类号：

071006 ;

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页码：5079 / 5079

页数：1

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[22] Roles of sodium channel SCN8A (Chr 12q13) and calcium channel CACNB4 (Chr 2q23) in human and mouse movement disorders
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[23] Three ENU-induced neurological mutations in the pore loop of sodium channel Scn8a (Nav1.6) and a genetically linked retinal mutation, rd13
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