Mutation screening of the PRRT2 gene for benign epilepsy with centrotemporal spikes in Chinese mainland population.

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Type and etiology of pediatric epilepsy in Jordan. A multi-center study.Sleep Related Epilepsy and Pharmacotherapy: An Insight

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Mutation screening of the PRRT2 gene for benign epilepsy with centrotemporal spikes in Chinese mainland population.

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2016 nî lūn-bûn

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2016年の論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年论文

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2016年论文

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2016年论文

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name

Mutation screening of the PRRT ...... n Chinese mainland population.

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Mutation screening of the PRRT ...... n Chinese mainland population.

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Mutation screening of the PRRT ...... n Chinese mainland population.

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Mutation screening of the PRRT ...... n Chinese mainland population.

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Mutation screening of the PRRT ...... n Chinese mainland population.

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Mutation screening of the PRRT ...... n Chinese mainland population.

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P1476

Mutation screening of the PRRT ...... n Chinese mainland population.

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Bei-Sha Tang

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

Hong Jiang

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

Kun Xia

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

Lu Shen

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

Nan Li

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

Xiang-Qian Che

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

Xiao Mao

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

Xin-Xiang Yan

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

Zhan-Fang Sun

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

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Exome sequencing identifies truncating mutations in PRRT2 that cause paroxysmal kinesigenic dyskinesia

Proposal for revised classification of epilepsies and epileptic syndromes. Commission on Classification and Terminology of the International League Against Epilepsy

PRRT2 mutations in familial infantile seizures, paroxysmal dyskinesia, and hemiplegic migraine.

PRRT2 gene mutations: from paroxysmal dyskinesia to episodic ataxia and hemiplegic migraine.

Clinical evaluation of idiopathic paroxysmal kinesigenic dyskinesia: new diagnostic criteria.

Identification of PRRT2 as the causative gene of paroxysmal kinesigenic dyskinesias.

Paroxysmal dyskinesias: clinical features and classification.

PRRT2 mutations in paroxysmal kinesigenic dyskinesia with infantile convulsions in a Taiwanese cohort.

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.

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10-13

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scholarly article

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10.3109/00207454.2015.1136886

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127

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2016-03-08T00:00:00Z

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26954261

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benign epilepsy with centrotemporal spikes

Mutation screening of the PRRT2 gene for benign epilepsy with centrotemporal spikes in Chinese mainland population.

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P2860

P2860

Mutation screening of the PRRT2 gene for benign epilepsy with centrotemporal spikes in Chinese mainland population.

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P921