Site-directed mutagenesis of neonatal convulsions associated KCNQ2 gene and its protein expression.

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Site-directed mutagenesis of neonatal convulsions associated KCNQ2 gene and its protein expression.

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2012 nî lūn-bûn

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2012年の論文

@ja

2012年論文

@yue

2012年論文

@zh-hant

2012年論文

@zh-hk

2012年論文

@zh-mo

2012年論文

@zh-tw

2012年论文

@wuu

2012年论文

@zh

2012年论文

@zh-cn

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Site-directed mutagenesis of n ...... ne and its protein expression.

@en

Site-directed mutagenesis of n ...... ne and its protein expression.

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Item

label

Site-directed mutagenesis of n ...... ne and its protein expression.

@en

Site-directed mutagenesis of n ...... ne and its protein expression.

@nl

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Site-directed mutagenesis of n ...... ne and its protein expression.

@en

Site-directed mutagenesis of n ...... ne and its protein expression.

@nl

P1476

Site-directed mutagenesis of n ...... ne and its protein expression.

@en

P2093

Hong-Xia Song

http://www.w3.org/2001/XMLSchema#string

Li Liu

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Rui-Ming Shi

http://www.w3.org/2001/XMLSchema#string

Wei Zhang

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Xi-Hui Zhou

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Zhi-Yan Hui

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P2860

A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family

A novel mutation in KCNQ2 gene causes benign familial neonatal convulsions in a Chinese family

A novel mutation in KCNQ2 associated with BFNC, drug resistant epilepsy, and mental retardation

Ion channel defects in idiopathic epilepsies.

Molecular pharmacology and therapeutic potential of neuronal Kv7-modulating drugs.

Functional analysis of novel KCNQ2 mutations found in patients with Benign Familial Neonatal Convulsions.

Lack of potassium current in W309R mutant KCNQ3 channel causing benign familial neonatal convulsions (BFNC).

A de novo KCNQ2 mutation detected in non-familial benign neonatal convulsions.

Altered KCNQ3 potassium channel function caused by the W309R pore-helix mutation found in human epilepsy.

Deletions or duplications in KCNQ2 can cause benign familial neonatal seizures.

P304

91-98

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P31

scholarly article

P356

10.3978/J.ISSN.2224-4336.2012.03.02

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P433

http://www.w3.org/2001/XMLSchema#string

P478

http://www.w3.org/2001/XMLSchema#string

P577

2012-10-01T00:00:00Z

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P698

26835270

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P932

4728876

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