Locus Heterogeneity in Epilepsy of Infancy with Migrating Focal Seizures.

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Locus Heterogeneity in Epilepsy of Infancy with Migrating Focal Seizures.

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2016 nî lūn-bûn

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2016年の論文

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年学术文章

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2016年學術文章

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2016年學術文章

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2016年學術文章

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Locus Heterogeneity in Epilepsy of Infancy with Migrating Focal Seizures.

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Locus Heterogeneity in Epilepsy of Infancy with Migrating Focal Seizures.

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prefLabel

Locus Heterogeneity in Epilepsy of Infancy with Migrating Focal Seizures.

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P1476

Locus Heterogeneity in Epilepsy of Infancy with Migrating Focal Seizures.

@en

P2860

Mutations in SLC12A5 in epilepsy of infancy with migrating focal seizures.

A variant of KCC2 from patients with febrile seizures impairs neuronal Cl- extrusion and dendritic spine formation

De novo gain-of-function KCNT1 channel mutations cause malignant migrating partial seizures of infancy.

SLC25A22 is a novel gene for migrating partial seizures in infancy.

Novel SCN1A mutation in a proband with malignant migrating partial seizures of infancy

SCN2A encephalopathy: A major cause of epilepsy of infancy with migrating focal seizures

Genetically encoded impairment of neuronal KCC2 cotransporter function in human idiopathic generalized epilepsy.

Hyperexcitability and epilepsy associated with disruption of the mouse neuronal-specific K-Cl cotransporter gene.

Early onset epileptic encephalopathy caused by de novo SCN8A mutations.

Migrating partial seizures in infancy: a malignant disorder with developmental arrest.

P304

43-45

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P31

scholarly article

P356

10.5698/1535-7597-16.1.43

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P407

English

P433

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

P478

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P50

Jennifer A Kearney

P577

2016-01-01T00:00:00Z

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P698

26900380

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P932

4749118

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