Significance of the SCN1A p.R1928G Change in Severe Myoclonic Epilepsy of Infancy

1 página.

Detalles Bibliográficos
Autores: Carranza, Daniel, Martínez Mir, Amalia, Macaya Ruiz, A.
Tipo de recurso: artículo
Fecha de publicación:2008
País:España
Institución:Consejo Superior de Investigaciones Científicas (CSIC)
Repositorio:DIGITAL.CSIC. Repositorio Institucional del CSIC
OAI Identifier:oai:digital.csic.es:10261/39257
Acceso en línea:http://hdl.handle.net/10261/39257
Access Level:acceso abierto
Palabra clave:Myoclonic epilepsy
Infancy
Dravet syndrome
SCN1A
Mutation
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spelling Significance of the SCN1A p.R1928G Change in Severe Myoclonic Epilepsy of InfancyCarranza, DanielMartínez Mir, AmaliaMacaya Ruiz, A.Myoclonic epilepsyInfancyDravet syndromeSCN1AMutation1 página.Reply to "Cryptogenic Epileptic Syndromes Related to SCN1A: Twelve Novel Mutations Idenfified"Peer reviewedAmerican Medical Association201120112008info:eu-repo/semantics/articlehttp://purl.org/coar/resource_type/c_6501http://hdl.handle.net/10261/39257reponame:DIGITAL.CSIC. Repositorio Institucional del CSICinstname:Consejo Superior de Investigaciones Científicas (CSIC)Ingléshttp://archneur.ama-assn.org/cgi/eletters/65/4/489#10208info:eu-repo/semantics/openAccessoai:digital.csic.es:10261/392572026-05-22T06:33:51Z
dc.title.none.fl_str_mv Significance of the SCN1A p.R1928G Change in Severe Myoclonic Epilepsy of Infancy
title Significance of the SCN1A p.R1928G Change in Severe Myoclonic Epilepsy of Infancy
spellingShingle Significance of the SCN1A p.R1928G Change in Severe Myoclonic Epilepsy of Infancy
Carranza, Daniel
Myoclonic epilepsy
Infancy
Dravet syndrome
SCN1A
Mutation
title_short Significance of the SCN1A p.R1928G Change in Severe Myoclonic Epilepsy of Infancy
title_full Significance of the SCN1A p.R1928G Change in Severe Myoclonic Epilepsy of Infancy
title_fullStr Significance of the SCN1A p.R1928G Change in Severe Myoclonic Epilepsy of Infancy
title_full_unstemmed Significance of the SCN1A p.R1928G Change in Severe Myoclonic Epilepsy of Infancy
title_sort Significance of the SCN1A p.R1928G Change in Severe Myoclonic Epilepsy of Infancy
dc.creator.none.fl_str_mv Carranza, Daniel
Martínez Mir, Amalia
Macaya Ruiz, A.
author Carranza, Daniel
author_facet Carranza, Daniel
Martínez Mir, Amalia
Macaya Ruiz, A.
author_role author
author2 Martínez Mir, Amalia
Macaya Ruiz, A.
author2_role author
author
dc.subject.none.fl_str_mv Myoclonic epilepsy
Infancy
Dravet syndrome
SCN1A
Mutation
topic Myoclonic epilepsy
Infancy
Dravet syndrome
SCN1A
Mutation
description 1 página.
publishDate 2008
dc.date.none.fl_str_mv 2008
2011
2011
dc.type.none.fl_str_mv info:eu-repo/semantics/article
http://purl.org/coar/resource_type/c_6501
format article
dc.identifier.none.fl_str_mv http://hdl.handle.net/10261/39257
url http://hdl.handle.net/10261/39257
dc.language.none.fl_str_mv Inglés
language_invalid_str_mv Inglés
dc.relation.none.fl_str_mv http://archneur.ama-assn.org/cgi/eletters/65/4/489#10208
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.publisher.none.fl_str_mv American Medical Association
publisher.none.fl_str_mv American Medical Association
dc.source.none.fl_str_mv reponame:DIGITAL.CSIC. Repositorio Institucional del CSIC
instname:Consejo Superior de Investigaciones Científicas (CSIC)
instname_str Consejo Superior de Investigaciones Científicas (CSIC)
reponame_str DIGITAL.CSIC. Repositorio Institucional del CSIC
collection DIGITAL.CSIC. Repositorio Institucional del CSIC
repository.name.fl_str_mv
repository.mail.fl_str_mv
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score 15.81155

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