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Author Correction: NEMF mutations that impair ribosome-associated quality control are associated with neuromuscular disease.
Martin, Paige B; Kigoshi-Tansho, Yu; Sher, Roger B; Ravenscroft, Gianina; Stauffer, Jennifer E; Kumar, Rajesh; Yonashiro, Ryo; Müller, Tina; Griffith, Christopher; Allen, William; Pehlivan, Davut; Harel, Tamar; Zenker, Martin; Howting, Denise; Schanze, Denny; Faqeih, Eissa A; Almontashiri, Naif A M; Maroofian, Reza; Houlden, Henry; Mazaheri, Neda; Galehdari, Hamid; Douglas, Ganka; Posey, Jennifer E; Ryan, Monique; Lupski, James R; Laing, Nigel G; Joazeiro, Claudio A P; Cox, Gregory A.
Afiliação
  • Martin PB; The Jackson Laboratory, Bar Harbor, ME, USA.
  • Kigoshi-Tansho Y; The University of Maine, Graduate School of Biomedical Science and Engineering, Orono, ME, USA.
  • Sher RB; Center for Molecular Biology of Heidelberg University (ZMBH), DKFZ-ZMBH Alliance, Heidelberg, Germany.
  • Ravenscroft G; Department of Neurobiology & Behavior, Stony Brook University, Stony Brook, NY, USA.
  • Stauffer JE; Center for Nervous System Disorders, Stony Brook University, Stony Brook, NY, USA.
  • Kumar R; Harry Perkins Institute of Medical Research, Centre for Medical Research, University of Western Australia, Nedlands, WA, Australia.
  • Yonashiro R; The Jackson Laboratory, Bar Harbor, ME, USA.
  • Müller T; Center for Molecular Biology of Heidelberg University (ZMBH), DKFZ-ZMBH Alliance, Heidelberg, Germany.
  • Griffith C; Department of Molecular Medicine, Scripps Research, Jupiter, FL, USA.
  • Allen W; Department of Molecular Medicine, Scripps Research, Jupiter, FL, USA.
  • Pehlivan D; College of Medicine Pediatrics, University of South Florida, Tampa, FL, USA.
  • Harel T; Mission Fullerton Genetics Center, Mission Health, Asheville, NC, USA.
  • Zenker M; Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX, USA.
  • Howting D; Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX, USA.
  • Schanze D; Department of Genetic and Metabolic Diseases, Hadassah-Hebrew University Medical Center, Jerusalem, Israel.
  • Faqeih EA; Institute of Human Genetics, Otto-von-Guericke University Magdeburg, Magdeburg, Germany.
  • Almontashiri NAM; Harry Perkins Institute of Medical Research, Centre for Medical Research, University of Western Australia, Nedlands, WA, Australia.
  • Maroofian R; Institute of Human Genetics, Otto-von-Guericke University Magdeburg, Magdeburg, Germany.
  • Houlden H; Department of Genetics, King Fahad Medical City, Riyadh, Saudi Arabia.
  • Mazaheri N; The Center for Genetics and Inherited Diseases, Taibah University, Almadinah Almunwarah, Saudi Arabia.
  • Galehdari H; Faculty of Applied Medical Sciences, Taibah University, Almadinah Almunwarah, Saudi Arabia.
  • Douglas G; Neurogenetics Laboratory, UCL Queen Square Institute of Neurology, London, UK.
  • Posey JE; The National Hospital for Neurology and Neurosurgery, London, UK.
  • Ryan M; Neurogenetics Laboratory, UCL Queen Square Institute of Neurology, London, UK.
  • Lupski JR; The National Hospital for Neurology and Neurosurgery, London, UK.
  • Laing NG; Department of Genetics, Faculty of Science, Shahid Chamran University of Ahvaz, Ahvaz, Iran.
  • Joazeiro CAP; Department of Genetics, Faculty of Science, Shahid Chamran University of Ahvaz, Ahvaz, Iran.
  • Cox GA; GeneDx, Inc, Gaithsberg, MD, USA.
Nat Commun ; 11(1): 5022, 2020 Oct 01.
Article em En | MEDLINE | ID: mdl-33004807
ABSTRACT
An amendment to this paper has been published and can be accessed via a link at the top of the paper.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Ano de publicação: 2020 Tipo de documento: Article
Texto completo
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PubMed Links
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Ano de publicação: 2020 Tipo de documento: Article