De Novo Mutations in YWHAG Cause Early-Onset Epilepsy-Reference-Cited by-同舟云学术

De Novo Mutations in YWHAG Cause Early-Onset Epilepsy

Published:2017-08 Issue:2 Volume:101 Page:300-310
ISSN:0002-9297
Container-title:The American Journal of Human Genetics
language:en
Short-container-title:The American Journal of Human Genetics

Author:

Guella Ilaria,McKenzie Marna B.,Evans Daniel M.,Buerki Sarah E.,Toyota Eric B.,Van Allen Margot I.,Suri Mohnish,Elmslie Frances,Simon Marleen E.H.,van Gassen Koen L.I.,Héron Delphine,Keren Boris,Nava Caroline,Connolly Mary B.,Demos Michelle,Farrer Matthew J.,Adam Shelin,Boelman Cyrus,Bolbocean Corneliu,Candido Tara,Eydoux Patrice,Horvath Gabriella,Huh Linda,Nelson Tanya N.,Sinclair Graham,van Karnebeek Clara,Vercauteren Suzanne

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics

Reference63 articles.

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2. Targeted resequencing in epileptic encephalopathies identifies de novo mutations in CHD2 and SYNGAP1;Carvill;Nat. Genet.,2013

3. De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy;Claes;Am. J. Hum. Genet.,2001

4. De novo mutations in epileptic encephalopathies;Allen;Nature,2013

5. De novo mutations in synaptic transmission genes including DNM1 cause epileptic encephalopathies;Am. J. Hum. Genet.,2014

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