Molecular genetics of human familial epilepsy syndromes.

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Mother and daughter with adolescent-onset severe frontal lobe dysfunction and epilepsy.

P2860

Q47131932-CBF44916-87CA-422E-9CC5-24F3D28C1FC7

P2860

Molecular genetics of human familial epilepsy syndromes.

Item

http://www.wikidata.org/entity/Q44182076

description

2002 nî lūn-bûn

@nan

2002年の論文

@ja

2002年学术文章

@wuu

2002年学术文章

@zh

2002年学术文章

@zh-cn

2002年学术文章

@zh-hans

2002年学术文章

@zh-my

2002年学术文章

@zh-sg

2002年學術文章

@yue

2002年學術文章

@zh-hant

name

Molecular genetics of human familial epilepsy syndromes.

@en

Molecular genetics of human familial epilepsy syndromes.

@nl

type

Item

label

Molecular genetics of human familial epilepsy syndromes.

@en

Molecular genetics of human familial epilepsy syndromes.

@nl

prefLabel

Molecular genetics of human familial epilepsy syndromes.

@en

Molecular genetics of human familial epilepsy syndromes.

@nl

P1476

Molecular genetics of human familial epilepsy syndromes.

@en

P2093

Akihisa Mitsudome

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

Motohiro Okada

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

Shinichi Hirose

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

Sunao Kaneko

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P2860

KCNQ2 and KCNQ3 potassium channel subunits: molecular correlates of the M-channel

Mutations of SCN1A, encoding a neuronal sodium channel, in two families with GEFS+2

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

Functional expression of two KvLQT1-related potassium channels responsible for an inherited idiopathic epilepsy

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

A potassium channel mutation in neonatal human epilepsy

Identification of a new locus for generalized epilepsy with febrile seizures plus (GEFS+) on chromosome 2q24-q33.

A second locus for familial generalized epilepsy with febrile seizures plus maps to chromosome 2q21-q33.

Autosomal dominant nocturnal frontal-lobe epilepsy: genetic heterogeneity and evidence for a second locus at 15q24

Coding and noncoding variation of the human calcium-channel beta4-subunit gene CACNB4 in patients with idiopathic generalized epilepsy and episodic ataxia.

P304

21-25

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P31

scholarly article

P356

10.1046/J.1528-1157.43.S.9.6.X

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P478

43 Suppl 9

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P577

2002-01-01T00:00:00Z

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P5875

8505899

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P698

12383275

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Molecular genetics of human familial epilepsy syndromes.

about

P2860

P2860

Molecular genetics of human familial epilepsy syndromes.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P478

P577

P5875

P698

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P478

P577

P5875

P698