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MAP1B mutations cause intellectual disability and extensive white matter deficit.
Walters, G Bragi; Gustafsson, Omar; Sveinbjornsson, Gardar; Eiriksdottir, Valgerdur K; Agustsdottir, Arna B; Jonsdottir, Gudrun A; Steinberg, Stacy; Gunnarsson, Arni F; Magnusson, Magnus I; Unnsteinsdottir, Unnur; Lee, Amy L; Jonasdottir, Adalbjorg; Sigurdsson, Asgeir; Jonasdottir, Aslaug; Skuladottir, Astros; Jonsson, Lina; Nawaz, Muhammad S; Sulem, Patrick; Frigge, Mike; Ingason, Andres; Love, Askell; Norddhal, Gudmundur L; Zervas, Mark; Gudbjartsson, Daniel F; Ulfarsson, Magnus O; Saemundsen, Evald; Stefansson, Hreinn; Stefansson, Kari.
Afiliação
  • Walters GB; deCODE genetics/Amgen, Reykjavik, 101, Iceland.
  • Gustafsson O; Faculty of Medicine, University of Iceland, Reykjavik, 101, Iceland.
  • Sveinbjornsson G; deCODE genetics/Amgen, Reykjavik, 101, Iceland.
  • Eiriksdottir VK; deCODE genetics/Amgen, Reykjavik, 101, Iceland.
  • Agustsdottir AB; deCODE genetics/Amgen, Reykjavik, 101, Iceland.
  • Jonsdottir GA; deCODE genetics/Amgen, Reykjavik, 101, Iceland.
  • Steinberg S; deCODE genetics/Amgen, Reykjavik, 101, Iceland.
  • Gunnarsson AF; deCODE genetics/Amgen, Reykjavik, 101, Iceland.
  • Magnusson MI; deCODE genetics/Amgen, Reykjavik, 101, Iceland.
  • Unnsteinsdottir U; deCODE genetics/Amgen, Reykjavik, 101, Iceland.
  • Lee AL; deCODE genetics/Amgen, Reykjavik, 101, Iceland.
  • Jonasdottir A; deCODE genetics/Amgen, Reykjavik, 101, Iceland.
  • Sigurdsson A; deCODE genetics/Amgen, Reykjavik, 101, Iceland.
  • Jonasdottir A; deCODE genetics/Amgen, Reykjavik, 101, Iceland.
  • Skuladottir A; deCODE genetics/Amgen, Reykjavik, 101, Iceland.
  • Jonsson L; deCODE genetics/Amgen, Reykjavik, 101, Iceland.
  • Nawaz MS; deCODE genetics/Amgen, Reykjavik, 101, Iceland.
  • Sulem P; Department of Pharmacology, Institute of Neuroscience and Physiology, Sahlgrenska Academy, University of Gothenburg, Gothenburg, 405 30, Sweden.
  • Frigge M; deCODE genetics/Amgen, Reykjavik, 101, Iceland.
  • Ingason A; Faculty of Medicine, University of Iceland, Reykjavik, 101, Iceland.
  • Love A; deCODE genetics/Amgen, Reykjavik, 101, Iceland.
  • Norddhal GL; deCODE genetics/Amgen, Reykjavik, 101, Iceland.
  • Zervas M; deCODE genetics/Amgen, Reykjavik, 101, Iceland.
  • Gudbjartsson DF; Faculty of Medicine, University of Iceland, Reykjavik, 101, Iceland.
  • Ulfarsson MO; Department of Radiology, Landspitali University Hospital, Fossvogur, Reykjavik, 108, Iceland.
  • Saemundsen E; deCODE genetics/Amgen, Reykjavik, 101, Iceland.
  • Stefansson H; deCODE genetics/Amgen, Reykjavik, 101, Iceland.
  • Stefansson K; deCODE genetics/Amgen, Reykjavik, 101, Iceland.
Nat Commun ; 9(1): 3456, 2018 08 27.
Article em En | MEDLINE | ID: mdl-30150678
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteína do X Frágil da Deficiência Intelectual / Substância Branca / Proteínas Associadas aos Microtúbulos Limite: Animals Idioma: En Revista: Nat Commun Assunto da revista: BIOLOGIA / CIENCIA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Islândia País de publicação: Reino Unido
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteína do X Frágil da Deficiência Intelectual / Substância Branca / Proteínas Associadas aos Microtúbulos Limite: Animals Idioma: En Revista: Nat Commun Assunto da revista: BIOLOGIA / CIENCIA Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Islândia País de publicação: Reino Unido