KCNK18 (TRESK) genetic variants in Italian patients with migraine.

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Genetic studies of Polish migraine patients: screening for causative mutations in four migraine-associated genes Ion channelopathies and migraine pathogenesis.

P2860

Q36446214-A031B3AD-6A71-40DB-941E-BBF9844418DA Q39227794-A15BF9C2-D7BC-4066-BC55-786DF85019D9

P2860

KCNK18 (TRESK) genetic variants in Italian patients with migraine.

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http://www.wikidata.org/entity/Q54188171

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2014 nî lūn-bûn

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2014年の論文

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2014年学术文章

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2014年学术文章

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2014年学术文章

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2014年学术文章

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2014年学术文章

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2014年學術文章

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2014年學術文章

@zh

2014年學術文章

@zh-hant

name

KCNK18 (TRESK) genetic variants in Italian patients with migraine.

@en

KCNK18

@nl

type

Item

label

KCNK18 (TRESK) genetic variants in Italian patients with migraine.

@en

KCNK18

@nl

prefLabel

KCNK18 (TRESK) genetic variants in Italian patients with migraine.

@en

KCNK18

@nl

P1476

KCNK18 (TRESK) genetic variants in Italian patients with migraine.

@en

P2093

Daniela Carli

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

Giorgio Dalla Volta

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

Innocenzo Rainero

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

Lidia Savi

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

Lorenzo Pinessi

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Paola Zavarise

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Pierpaola Fenoglio

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Salvatore Gallone

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Salvatore Gentile

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

Silvia Boschi

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P2860

Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump alpha2 subunit associated with familial hemiplegic migraine type 2

A novel two-pore domain K+ channel, TRESK, is localized in the spinal cord

Functional analysis of missense variants in the TRESK (KCNK18) K channel

Mutation in the neuronal voltage-gated sodium channel SCN1A in familial hemiplegic migraine

Familial hemiplegic migraine and episodic ataxia type-2 are caused by mutations in the Ca2+ channel gene CACNL1A4

A dominant-negative mutation in the TRESK potassium channel is linked to familial migraine with aura.

Discrete change in volatile anesthetic sensitivity in mice with inactivated tandem pore potassium ion channel TRESK.

Predicting the insurgence of human genetic diseases associated to single point protein mutations with support vector machines and evolutionary information.

SNAP: predict effect of non-synonymous polymorphisms on function.

Epilepsy and migraine.

P304

1515-1522

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P31

scholarly article

P356

10.1111/HEAD.12439

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P433

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

P478

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

P50

Elisa Rubino

Paolo Benna

P577

2014-10-01T00:00:00Z

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P5875

266972320

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P698

25324165

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P921

migraine disorder

An Eadailt

KCNK18 (TRESK) genetic variants in Italian patients with migraine.

about

P2860

P2860

KCNK18 (TRESK) genetic variants in Italian patients with migraine.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P5875

P698

P921

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P50

P577

P5875

P698

P921