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Pathophysiology of KCNQ channels: Neonatal epilepsy and progressive deafness
被引:34
作者
:
Jentsch, TJ
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Hamburg, Zentrum Mol Neurobiol Hamburg, Hamburg, Germany
Univ Hamburg, Zentrum Mol Neurobiol Hamburg, Hamburg, Germany
Jentsch, TJ
[
1
]
Schroeder, BC
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Hamburg, Zentrum Mol Neurobiol Hamburg, Hamburg, Germany
Univ Hamburg, Zentrum Mol Neurobiol Hamburg, Hamburg, Germany
Schroeder, BC
[
1
]
Kubisch, C
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Hamburg, Zentrum Mol Neurobiol Hamburg, Hamburg, Germany
Univ Hamburg, Zentrum Mol Neurobiol Hamburg, Hamburg, Germany
Kubisch, C
[
1
]
Friedrich, T
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Hamburg, Zentrum Mol Neurobiol Hamburg, Hamburg, Germany
Univ Hamburg, Zentrum Mol Neurobiol Hamburg, Hamburg, Germany
Friedrich, T
[
1
]
Stein, V
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Hamburg, Zentrum Mol Neurobiol Hamburg, Hamburg, Germany
Univ Hamburg, Zentrum Mol Neurobiol Hamburg, Hamburg, Germany
Stein, V
[
1
]
机构
:
[1]
Univ Hamburg, Zentrum Mol Neurobiol Hamburg, Hamburg, Germany
来源
:
EPILEPSIA
|
2000年
/ 41卷
/ 08期
关键词
:
D O I
:
10.1111/j.1528-1157.2000.tb00302.x
中图分类号
:
R74 [神经病学与精神病学];
学科分类号
:
摘要
:
[No abstract available]
引用
收藏
页码:1068 / 1069
页数:2
相关论文
共 9 条
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A potassium channel mutation in neonatal human epilepsy
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0
引用数:
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h-index:
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机构:
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h-index:
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h-index:
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机构:
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论文数:
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h-index:
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Propping, P
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0
引用数:
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h-index:
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Jentsch, TJ
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引用数:
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h-index:
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h-index:
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279
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A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family
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论文数:
0
引用数:
0
h-index:
0
机构:
Univ Utah, Dept Human Genet, Salt Lake City, UT 84112 USA
Charlier, C
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Singh, NA
论文数:
0
引用数:
0
h-index:
0
机构:
Univ Utah, Dept Human Genet, Salt Lake City, UT 84112 USA
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Ryan, SG
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引用数:
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h-index:
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机构:
Univ Utah, Dept Human Genet, Salt Lake City, UT 84112 USA
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h-index:
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机构:
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h-index:
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Schroeder, BC
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h-index:
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