Somatosensory reflex seizures in a child with epilepsy related to novel SCN1A mutation.

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Somatosensory reflex seizures in a child with epilepsy related to novel SCN1A mutation.

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http://www.wikidata.org/entity/Q47790206

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2016 nî lūn-bûn

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2016年の論文

@ja

2016年学术文章

@wuu

2016年学术文章

@zh

2016年学术文章

@zh-cn

2016年学术文章

@zh-hans

2016年学术文章

@zh-my

2016年学术文章

@zh-sg

2016年學術文章

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2016年學術文章

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Somatosensory reflex seizures in a child with epilepsy related to novel SCN1A mutation.

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Somatosensory reflex seizures in a child with epilepsy related to novel SCN1A mutation.

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Item

label

Somatosensory reflex seizures in a child with epilepsy related to novel SCN1A mutation.

@en

Somatosensory reflex seizures in a child with epilepsy related to novel SCN1A mutation.

@nl

prefLabel

Somatosensory reflex seizures in a child with epilepsy related to novel SCN1A mutation.

@en

Somatosensory reflex seizures in a child with epilepsy related to novel SCN1A mutation.

@nl

P1476

Somatosensory reflex seizures in a child with epilepsy related to novel SCN1A mutation.

@en

P2093

Dilek Cavusoglu

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Nihal Olgac Dundar

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

Pinar Arican

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

Pinar Gencpinar

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

Taha Resid Ozdemır

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P2860

De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy

Spectrum of phenotypes in female patients with epilepsy due to protocadherin 19 mutations.

Dravet syndrome as epileptic encephalopathy: evidence from long-term course and neuropathology.

A catalog of SCN1A variants.

Borderline Dravet syndrome: a useful diagnostic category?

The genetics of Dravet syndrome.

Dravet syndrome: the main issues.

The SCN1A mutation database: updating information and analysis of the relationships among genotype, functional alteration, and phenotype.

Dravet syndrome

Acute encephalopathy with a truncation mutation in the SCN1A gene: a case report.

P2888

s00381-016-3297-6

P304

677-680

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P31

scholarly article

P356

10.1007/S00381-016-3297-6

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P433

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

P478

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P577

2016-11-26T00:00:00Z

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P698

27889818

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