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Ethical, legal, and social dimensions of epilepsy genetics.

Ethical, legal, and social dimensions of epilepsy genetics.

http://www.wikidata.org/entity/Q34575712

about

Genetic testing in the epilepsies--report of the ILAE Genetics Commission Genetic testing in the epilepsies-developments and dilemmas.What's at stake? Genetic information from the perspective of people with epilepsy and their family members.Genetic causal attribution of epilepsy and its implications for felt stigma.Role of genetics in the diagnosis and treatment of epilepsy.Depression and genetic causal attribution of epilepsy in multiplex epilepsy families From genetics to genomics of epilepsy.Genetics of Epilepsy in Clinical Practice.The clinical utility of an SCN1A genetic diagnosis in infantile-onset epilepsy.Return of individual results in epilepsy genomic research: A view from the field

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Ethical, legal, and social dimensions of epilepsy genetics.

http://www.wikidata.org/entity/Q34575712

description

2006 nî lūn-bûn

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2006 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2006 թվականի հոտեմբերին հրատարակված գիտական հոդված

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2006年の論文

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2006年学术文章

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2006年学术文章

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2006年学术文章

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2006年学术文章

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2006年学术文章

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2006年學術文章

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name

Ethical, legal, and social dimensions of epilepsy genetics.

@ast

Ethical, legal, and social dimensions of epilepsy genetics.

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Ethical, legal, and social dimensions of epilepsy genetics.

@nl

type

label

Ethical, legal, and social dimensions of epilepsy genetics.

@ast

Ethical, legal, and social dimensions of epilepsy genetics.

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Ethical, legal, and social dimensions of epilepsy genetics.

@nl

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Ethical, legal, and social dimensions of epilepsy genetics.

@ast

Ethical, legal, and social dimensions of epilepsy genetics.

@en

Ethical, legal, and social dimensions of epilepsy genetics.

@nl

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J.1528-1167.2006.00632.X

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Ethical, legal, and social dimensions of epilepsy genetics.

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Sara Shostak

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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

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

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

LGI1 mutations in autosomal dominant partial epilepsy with auditory features.

A missense mutation of the Na+ channel alpha II subunit gene Na(v)1.2 in a patient with febrile and afebrile seizures causes channel dysfunction

Truncation of the GABA(A)-receptor gamma2 subunit in a family with generalized epilepsy with febrile seizures plus

Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features

A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family

The nicotinic receptor beta 2 subunit is mutant in nocturnal frontal lobe epilepsy

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scholarly article

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10.1111/J.1528-1167.2006.00632.X

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10

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17054679

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research ethics

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1802101

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