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A novel CHCHD10 mutation implicates a Mia40-dependent mitochondrial import deficit in ALS.
Lehmer, Carina; Schludi, Martin H; Ransom, Linnea; Greiling, Johanna; Junghänel, Michaela; Exner, Nicole; Riemenschneider, Henrick; van der Zee, Julie; Van Broeckhoven, Christine; Weydt, Patrick; Heneka, Michael T; Edbauer, Dieter.
Afiliação
  • Lehmer C; German Center for Neurodegenerative Diseases (DZNE) Munich, Munich, Germany.
  • Schludi MH; German Center for Neurodegenerative Diseases (DZNE) Munich, Munich, Germany.
  • Ransom L; Munich Cluster for Systems Neurology (SyNergy), Munich, Germany.
  • Greiling J; German Center for Neurodegenerative Diseases (DZNE) Munich, Munich, Germany.
  • Junghänel M; German Center for Neurodegenerative Diseases (DZNE) Munich, Munich, Germany.
  • Exner N; German Center for Neurodegenerative Diseases (DZNE) Munich, Munich, Germany.
  • Riemenschneider H; Biomedical Center (BMC), Biochemistry, Ludwig-Maximilians-Universität München, Munich, Germany.
  • van der Zee J; German Center for Neurodegenerative Diseases (DZNE) Munich, Munich, Germany.
  • Van Broeckhoven C; Neurodegenerative Brain Diseases Group, Center for Molecular Neurology, VIB, Antwerp, Belgium.
  • Weydt P; Laboratory of Neurogenetics, Institute Born-Bunge, University of Antwerp, Antwerp, Belgium.
  • Heneka MT; Neurodegenerative Brain Diseases Group, Center for Molecular Neurology, VIB, Antwerp, Belgium.
  • Edbauer D; Laboratory of Neurogenetics, Institute Born-Bunge, University of Antwerp, Antwerp, Belgium.
EMBO Mol Med ; 10(6)2018 06.
Article em En | MEDLINE | ID: mdl-29789341
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteínas Mitocondriais / Esclerose Lateral Amiotrófica Limite: Adult / Humans Idioma: En Revista: EMBO Mol Med Assunto da revista: BIOLOGIA MOLECULAR Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Alemanha
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Proteínas Mitocondriais / Esclerose Lateral Amiotrófica Limite: Adult / Humans Idioma: En Revista: EMBO Mol Med Assunto da revista: BIOLOGIA MOLECULAR Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Alemanha