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Genetic basis of pediatric epilepsy syndromes.

Genetic basis of pediatric epilepsy syndromes.

http://www.wikidata.org/entity/Q33723915

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Genetic basis of pediatric epilepsy syndromes.

http://www.wikidata.org/entity/Q33723915

description

2017 nî lūn-bûn

@nan

2017 թուականի Մարտին հրատարակուած գիտական յօդուած

@hyw

2017 թվականի մարտին հրատարակված գիտական հոդված

@hy

2017年の論文

@ja

2017年論文

@yue

2017年論文

@zh-hant

2017年論文

@zh-hk

2017年論文

@zh-mo

2017年論文

@zh-tw

2017年论文

@wuu

name

Genetic basis of pediatric epilepsy syndromes.

@ast

Genetic basis of pediatric epilepsy syndromes.

@en

type

label

Genetic basis of pediatric epilepsy syndromes.

@ast

Genetic basis of pediatric epilepsy syndromes.

@en

prefLabel

Genetic basis of pediatric epilepsy syndromes.

@ast

Genetic basis of pediatric epilepsy syndromes.

@en

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Experimental and Therapeutic Medicine

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Genetic basis of pediatric epilepsy syndromes.

@en

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Dongli Zhang

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

Xiaoming Liu

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

Xingqiang Deng

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P2860

A missense mutation in the neuronal nicotinic acetylcholine receptor alpha 4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy

De novo loss-of-function mutations in CHD2 cause a fever-sensitive myoclonic epileptic encephalopathy sharing features with Dravet syndrome

Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1.

A missense mutation of the Na+ channel alpha II subunit gene Na(v)1.2 in a patient with febrile and afebrile seizures causes channel dysfunction

Genetic epilepsy syndromes without structural brain abnormalities: clinical features and experimental models

Epileptic encephalopathies: new genes and new pathways

Epilepsy and chromosome 18 abnormalities: A review

De novo pathogenic SCN8A mutation identified by whole-genome sequencing of a family quartet affected by infantile epileptic encephalopathy and SUDEP

Mutations of sodium channel alpha subunit type 1 (SCN1A) in intractable childhood epilepsies with frequent generalized tonic-clonic seizures

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

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2129-2133

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scholarly article

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10.3892/ETM.2017.4267

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5

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13

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2017-03-27T00:00:00Z

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5443213

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