Genetic and epigenetic mechanisms of epilepsy: a review.

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The Metabotropic Purinergic P2Y Receptor Family as Novel Drug Target in Epilepsy.APOE hypermethylation is associated with autism spectrum disorder in a Chinese population.

P2860

Q55137379-CD6B0407-DDC2-47F3-A270-1C607AB37062 Q55228994-E32A86A7-92C6-401B-BA42-D1CCAB35F7EC

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Genetic and epigenetic mechanisms of epilepsy: a review.

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http://www.wikidata.org/entity/Q41057615

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2017 nî lūn-bûn

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2017年の論文

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2017年学术文章

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2017年学术文章

@zh-cn

2017年学术文章

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2017年学术文章

@zh-my

2017年学术文章

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2017年學術文章

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2017年學術文章

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2017年學術文章

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Genetic and epigenetic mechanisms of epilepsy: a review.

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Genetic and epigenetic mechanisms of epilepsy: a review.

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Genetic and epigenetic mechanisms of epilepsy: a review.

@en

P1476

Genetic and epigenetic mechanisms of epilepsy: a review.

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Mohan Giri

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

Tian Chen

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

Yadu Nanda Subedi

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

Yan Li

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

Zhenyi Xia

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P2860

Overview of the voltage-gated sodium channel family

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

CHRNB2 is the second acetylcholine receptor subunit associated with autosomal dominant nocturnal frontal lobe epilepsy

TBC1D24, an ARF6-interacting protein, is mutated in familial infantile myoclonic epilepsy

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

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

A homozygous mutation in human PRICKLE1 causes an autosomal-recessive progressive myoclonus epilepsy-ataxia syndrome

A polymorphism in CALHM1 influences Ca2+ homeostasis, Abeta levels, and Alzheimer's disease risk

BRD2 (RING3) is a probable major susceptibility gene for common juvenile myoclonic epilepsy

Benign familial infantile convulsions: mapping of a novel locus on chromosome 2q24 and evidence for genetic heterogeneity

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1841-1859

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scholarly article

P356

10.2147/NDT.S142032

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English

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2017-07-13T00:00:00Z

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28761347

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P932

5516882

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Genetic and epigenetic mechanisms of epilepsy: a review.

about

P2860

P2860

Genetic and epigenetic mechanisms of epilepsy: a review.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P478

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P478

P577

P698

P932