Genetics of epilepsy: The testimony of twins in the molecular era - Wikidata - awgldk - TriplyDB

Genetics of epilepsy: The testimony of twins in the molecular era

Genetics of epilepsy: The testimony of twins in the molecular era

http://www.wikidata.org/entity/Q34198753

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Burden analysis of rare microdeletions suggests a strong impact of neurodevelopmental genes in genetic generalised epilepsies A practical, simple, and useful method of categorizing interictal EEG features in children.A microRNA-328 binding site in PAX6 is associated with centrotemporal spikes of rolandic epilepsy.Primer Part 1-The building blocks of epilepsy genetics.Heterogeneous contribution of microdeletions in the development of common generalised and focal epilepsies.Phenotypic analysis of 303 multiplex families with common epilepsies.Classification of the epilepsies: New concepts for discussion and debate-Special report of the ILAE Classification Task Force of the Commission for Classification and Terminology.

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Genetics of epilepsy: The testimony of twins in the molecular era

http://www.wikidata.org/entity/Q34198753

description

2014 nî lūn-bûn

@nan

2014 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի օգոստոսին հրատարակված գիտական հոդված

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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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name

Genetics of epilepsy: The testimony of twins in the molecular era

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Genetics of epilepsy: The testimony of twins in the molecular era

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Genetics of epilepsy: The testimony of twins in the molecular era

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Genetics of epilepsy: The testimony of twins in the molecular era

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Genetics of epilepsy: The testimony of twins in the molecular era

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Genetics of epilepsy: The testimony of twins in the molecular era

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Genetics of epilepsy: The testimony of twins in the molecular era

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Genetics of epilepsy: The testimony of twins in the molecular era

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Genetics of epilepsy: The testimony of twins in the molecular era

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Jazmin Eckhaus

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John C Mulley

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Lata Vadlamudi

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P2860

LGI1 mutations in autosomal dominant partial epilepsy with auditory features.

Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1.

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

Glucose transporter 1 deficiency in the idiopathic generalized epilepsies

Severe myoclonic epilepsy of infancy: extended spectrum of GEFS+?

Generalized epilepsy with febrile seizures plus. A genetic disorder with heterogeneous clinical phenotypes

Proposal for revised classification of epilepsies and epileptic syndromes. Commission on Classification and Terminology of the International League Against Epilepsy

Revised terminology and concepts for organization of seizures and epilepsies: report of the ILAE Commission on Classification and Terminology, 2005-2009

Mutations in DEPDC5 cause familial focal epilepsy with variable foci

Epilepsy in twins: insights from unique historical data of William Lennox.

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