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Correction to: The CAPOS mutation in ATP1A3 alters Na/K-ATPase function and results in auditory neuropathy which has implications for management.
Tranebjærg, Lisbeth; Strenzke, Nicola; Lindholm, Sture; Rendtorff, Nanna D; Poulsen, Hanne; Khandelia, Himanshu; Kopec, Wojciech; Lyngbye, Troels J Brünnich; Hamel, Christian; Delettre, Cecile; Bocquet, Beatrice; Bille, Michael; Owen, Hanne H; Bek, Toke; Jensen, Hanne; Østergaard, Karen; Möller, Claes; Luxon, Linda; Carr, Lucinda; Wilson, Louise; Rajput, Kaukab; Sirimanna, Tony; Harrop-Griffiths, Katherine; Rahman, Shamima; Vona, Barbara; Doll, Julia; Haaf, Thomas; Bartsch, Oliver; Rosewich, Hendrik; Moser, Tobias; Bitner-Glindzicz, Maria.
Afiliación
  • Tranebjærg L; Department of Otorhinolaryngology, Head and Neck Surgery and Audiology, Rigshospitalet/Bispebjerg, Copenhagen, Denmark. tranebjaerg@sund.ku.dk.
  • Strenzke N; Department of Clinical Genetics, The Kennedy Center, Copenhagen University Hospital, Copenhagen, Denmark. tranebjaerg@sund.ku.dk.
  • Lindholm S; Institute of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark. tranebjaerg@sund.ku.dk.
  • Rendtorff ND; Auditory Systems Physiology Group, InnerEarLab, Department of Otolaryngology, University Medical Center, Göttingen, Germany.
  • Poulsen H; ENT-Department, County Hospital Kalmar, Kalmar, Sweden.
  • Khandelia H; Department of Clinical Genetics, The Kennedy Center, Copenhagen University Hospital, Copenhagen, Denmark.
  • Kopec W; Institute of Biomedicine, University of Aarhus, Aarhus, Denmark.
  • Lyngbye TJB; MEMPHYS-Center for Biomembrane Physics, University of Southern Denmark, Odense, Denmark.
  • Hamel C; MEMPHYS-Center for Biomembrane Physics, University of Southern Denmark, Odense, Denmark.
  • Delettre C; Computational Biomolecular Dynamics Group, Max Planck Institute for Biophysical Chemistry, Göttingen, Germany.
  • Bocquet B; Pediatric Department, Aarhus University Hospital, Aarhus, Denmark.
  • Bille M; Maladies Sensorielles Genetiques, CHRU, Montpellier, France.
  • Owen HH; INSERM U1051, Institute for Neurosciences of Montpellier, Montpellier, France.
  • Bek T; Universite Montpellier, Montpellier, France.
  • Jensen H; INSERM U1051, Institute for Neurosciences of Montpellier, Montpellier, France.
  • Østergaard K; Universite Montpellier, Montpellier, France.
  • Möller C; Maladies Sensorielles Genetiques, CHRU, Montpellier, France.
  • Luxon L; INSERM U1051, Institute for Neurosciences of Montpellier, Montpellier, France.
  • Carr L; Universite Montpellier, Montpellier, France.
  • Wilson L; Department of Otorhinolaryngology, Head and Neck Surgery and Audiology, Rigshospitalet/Gentofte Hospital, Hellerup, Denmark.
  • Rajput K; Department of Audiology, Aarhus University Hospital, Aarhus, Denmark.
  • Sirimanna T; Department of Ophthalmology, Aarhus University Hospital, Aarhus, Denmark.
  • Harrop-Griffiths K; Eye Department Glostrup Hospital, Rigshospitalet, The Kennedy Centre, Glostrup, Denmark.
  • Rahman S; Department of Neurology, Aarhus University Hospital and University of Aarhus, Aarhus, Denmark.
  • Vona B; Audiological Research Centre, Faculty of Medicine and Health, Örebro University, Örebro, Sweden.
  • Doll J; Department of Neurotology, National Hospital for Neurology, Queen Square, London, WC1N 3BG, UK.
  • Haaf T; Department of Neurology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, WC1N 3JH, UK.
  • Bartsch O; North East Thames Regional Genetics Service, Great Ormond Street Hospital for Children NHS Foundation Trust, London, WC1N 3JH, UK.
  • Rosewich H; Cochlear Implant Department, Great Ormond Street Hospital for Children NHS Foundation Trust, London, WC1N 3JH, UK.
  • Moser T; Department of Audiovestibular Medicine, Great Ormond Street Hospital for Children NHS Foundation Trust, London, WC1N 3JH, UK.
  • Bitner-Glindzicz M; Nuffield Hearing and Speech Centre, Royal National Throat Nose and Ear Hospital, London, WC1X 8DA, UK.
Hum Genet ; 137(3): 279-280, 2018 03.
Article en En | MEDLINE | ID: mdl-29435658
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Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Hum Genet Año: 2018 Tipo del documento: Article País de afiliación: Dinamarca
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Bases de datos: MEDLINE Idioma: En Revista: Hum Genet Año: 2018 Tipo del documento: Article País de afiliación: Dinamarca