Genetic analysis of benign familial epilepsies in the first year of life in a Chinese cohort.

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Genetic analysis of benign familial epilepsies in the first year of life in a Chinese cohort.

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

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2017年学术文章

@zh-cn

2017年学术文章

@zh-hans

2017年学术文章

@zh-my

2017年学术文章

@zh-sg

2017年學術文章

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2017年學術文章

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Genetic analysis of benign fam ...... r of life in a Chinese cohort.

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Genetic analysis of benign fam ...... r of life in a Chinese cohort.

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label

Genetic analysis of benign fam ...... r of life in a Chinese cohort.

@en

Genetic analysis of benign fam ...... r of life in a Chinese cohort.

@nl

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Genetic analysis of benign fam ...... r of life in a Chinese cohort.

@en

Genetic analysis of benign fam ...... r of life in a Chinese cohort.

@nl

P1476

Genetic analysis of benign fam ...... r of life in a Chinese cohort.

@en

P2093

Aijie Liu

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Jing Zhang

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

Liping Wei

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

Qi Zeng

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Xiaoling Yang

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

Xiaoyan Liu

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Xiru Wu

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

Ye Wu

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Yuehua Zhang

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Zhixian Yang

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P2860

A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns

Familial infantile convulsions and paroxysmal choreoathetosis: a new neurological syndrome linked to the pericentromeric region of human chromosome 16

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

Sodium-channel defects in benign familial neonatal-infantile seizures

KCNQ2 and KCNQ3 potassium channel genes in benign familial neonatal convulsions: expansion of the functional and mutation spectrum

Benign familial neonatal-infantile seizures: characterization of a new sodium channelopathy

Contiguous deletion of KCNQ2 and CHRNA4 may cause a different disorder from benign familial neonatal seizures.

Phenotypes and PRRT2 mutations in Chinese families with benign familial infantile epilepsy and infantile convulsions with paroxysmal choreoathetosis

PRRT2 mutations cause benign familial infantile epilepsy and infantile convulsions with choreoathetosis syndrome.

Mutations in the gene PRRT2 cause paroxysmal kinesigenic dyskinesia with infantile convulsions.

P2888

s10038-017-0359-x

P304

9-18

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P31

scholarly article

P356

10.1038/S10038-017-0359-X

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P433

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P478

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P577

2017-11-13T00:00:00Z

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P698

29215089

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