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Analysis of shared common genetic risk between amyotrophic lateral sclerosis and epilepsy.
Schijven, Dick; Stevelink, Remi; McCormack, Mark; van Rheenen, Wouter; Luykx, Jurjen J; Koeleman, Bobby P C; Veldink, Jan H.
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  • Schijven D; Department of Neurology and Neurosurgery, UMC Utrecht Brain Center, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands; Department of Psychiatry, UMC Utrecht Brain Center, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands; Department of Tran
  • Stevelink R; Center for Molecular Medicine, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.
  • McCormack M; Center for Molecular Medicine, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands; Department of Molecular and Cellular Therapeutics, The Royal College of Surgeons in Ireland, Dublin, Ireland.
  • van Rheenen W; Department of Neurology and Neurosurgery, UMC Utrecht Brain Center, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.
  • Luykx JJ; Department of Psychiatry, UMC Utrecht Brain Center, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.
  • Koeleman BPC; Center for Molecular Medicine, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands.
  • Veldink JH; Department of Neurology and Neurosurgery, UMC Utrecht Brain Center, University Medical Center Utrecht, Utrecht University, Utrecht, the Netherlands. Electronic address: j.h.veldink@umcutrecht.nl.
Neurobiol Aging ; 92: 153.e1-153.e5, 2020 08.
Article en En | MEDLINE | ID: mdl-32409253
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Variación Genética / Epilepsia / Estudio de Asociación del Genoma Completo / Resultados Negativos / Esclerosis Amiotrófica Lateral Límite: Humans Idioma: En Revista: Neurobiol Aging Año: 2020 Tipo del documento: Article
Texto completo
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Variación Genética / Epilepsia / Estudio de Asociación del Genoma Completo / Resultados Negativos / Esclerosis Amiotrófica Lateral Límite: Humans Idioma: En Revista: Neurobiol Aging Año: 2020 Tipo del documento: Article