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Tranebjærg L, Strenzke N, Lindholm S, et al. Correction to: The CAPOS mutation in ATP1A3 alters Na/K-ATPase function and results in auditory neuropathy which has implications for management. Hum Genet. 2018;137(3):279-280doi: 10.1007/s00439-018-1870-7.
Tranebjærg, L., Strenzke, N., Lindholm, S., Rendtorff, N. D., Poulsen, H., Khandelia, H., Kopec, W., Lyngbye, T. J. B., Hamel, C., Delettre, C., Bocquet, B., Bille, M., Owen, H. H., Bek, T., Jensen, H., Østergaard, K., Möller, C., Luxon, L., Carr, L., Wilson, L., Rajput, K., Sirimanna, T., Harrop-Griffiths, K., Rahman, S., Vona, B., Doll, J., Haaf, T., Bartsch, O., Rosewich, H., Moser, T., & Bitner-Glindzicz, M. (2018). Correction to: The CAPOS mutation in ATP1A3 alters Na/K-ATPase function and results in auditory neuropathy which has implications for management. Human genetics, 137(3), 279-280. https://doi.org/10.1007/s00439-018-1870-7
Tranebjærg, Lisbeth, et al. "Correction to: The CAPOS mutation in ATP1A3 alters Na/K-ATPase function and results in auditory neuropathy which has implications for management." Human genetics vol. 137,3 (2018): 279-280. doi: https://doi.org/10.1007/s00439-018-1870-7
Tranebjærg L, Strenzke N, Lindholm S, Rendtorff ND, Poulsen H, Khandelia H, Kopec W, Lyngbye TJB, Hamel C, Delettre C, Bocquet B, Bille M, Owen HH, Bek T, Jensen H, Østergaard K, Möller C, Luxon L, Carr L, Wilson L, Rajput K, Sirimanna T, Harrop-Griffiths K, Rahman S, Vona B, Doll J, Haaf T, Bartsch O, Rosewich H, Moser T, Bitner-Glindzicz M. Correction to: The CAPOS mutation in ATP1A3 alters Na/K-ATPase function and results in auditory neuropathy which has implications for management. Hum Genet. 2018 Mar;137(3):279-280. doi: 10.1007/s00439-018-1870-7. PMID: 29435658.
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Hum Genet. 2018 Mar;137(3):279-280. doi: 10.1007/s00439-018-1870-7.

Correction to: The CAPOS mutation in ATP1A3 alters Na/K-ATPase function and results in auditory neuropathy which has implications for management.

Human genetics

Lisbeth Tranebjærg, Nicola Strenzke, Sture Lindholm, Nanna D Rendtorff, Hanne Poulsen, Himanshu Khandelia, Wojciech Kopec, Troels J Brünnich Lyngbye, Christian Hamel, Cecile Delettre, Beatrice Bocquet, Michael Bille, Hanne H Owen, Toke Bek, Hanne Jensen, Karen Østergaard, Claes Möller, Linda Luxon, Lucinda Carr, Louise Wilson, Kaukab Rajput, Tony Sirimanna, Katherine Harrop-Griffiths, Shamima Rahman, Barbara Vona, Julia Doll, Thomas Haaf, Oliver Bartsch, Hendrik Rosewich, Tobias Moser, Maria Bitner-Glindzicz

Affiliations

  1. Department of Otorhinolaryngology, Head and Neck Surgery and Audiology, Rigshospitalet/Bispebjerg, Copenhagen, Denmark. [email protected].
  2. Department of Clinical Genetics, The Kennedy Center, Copenhagen University Hospital, Copenhagen, Denmark. [email protected].
  3. Institute of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark. [email protected].
  4. Auditory Systems Physiology Group, InnerEarLab, Department of Otolaryngology, University Medical Center, Göttingen, Germany.
  5. ENT-Department, County Hospital Kalmar, Kalmar, Sweden.
  6. Department of Clinical Genetics, The Kennedy Center, Copenhagen University Hospital, Copenhagen, Denmark.
  7. Institute of Biomedicine, University of Aarhus, Aarhus, Denmark.
  8. MEMPHYS-Center for Biomembrane Physics, University of Southern Denmark, Odense, Denmark.
  9. Computational Biomolecular Dynamics Group, Max Planck Institute for Biophysical Chemistry, Göttingen, Germany.
  10. Pediatric Department, Aarhus University Hospital, Aarhus, Denmark.
  11. Maladies Sensorielles Genetiques, CHRU, Montpellier, France.
  12. INSERM U1051, Institute for Neurosciences of Montpellier, Montpellier, France.
  13. Universite Montpellier, Montpellier, France.
  14. Department of Otorhinolaryngology, Head and Neck Surgery and Audiology, Rigshospitalet/Gentofte Hospital, Hellerup, Denmark.
  15. Department of Audiology, Aarhus University Hospital, Aarhus, Denmark.
  16. Department of Ophthalmology, Aarhus University Hospital, Aarhus, Denmark.
  17. Eye Department Glostrup Hospital, Rigshospitalet, The Kennedy Centre, Glostrup, Denmark.
  18. Department of Neurology, Aarhus University Hospital and University of Aarhus, Aarhus, Denmark.
  19. Audiological Research Centre, Faculty of Medicine and Health, Örebro University, Örebro, Sweden.
  20. Department of Neurotology, National Hospital for Neurology, Queen Square, London, WC1N 3BG, UK.
  21. Department of Neurology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, WC1N 3JH, UK.
  22. North East Thames Regional Genetics Service, Great Ormond Street Hospital for Children NHS Foundation Trust, London, WC1N 3JH, UK.
  23. Cochlear Implant Department, Great Ormond Street Hospital for Children NHS Foundation Trust, London, WC1N 3JH, UK.
  24. Department of Audiovestibular Medicine, Great Ormond Street Hospital for Children NHS Foundation Trust, London, WC1N 3JH, UK.
  25. Nuffield Hearing and Speech Centre, Royal National Throat Nose and Ear Hospital, London, WC1X 8DA, UK.
  26. Genetic and Genomic Medicine Programme, UCL Great Ormond Street Institute of Child Health, London, WC1N 1EH, UK.
  27. Institute of Human Genetics, Julius Maximilians University Würzburg, Würzburg, Germany.
  28. University Medical Centre, Institute of Human Genetics, Johannes Gutenberg University Mainz, Langenbeckstrasse 1, Mainz, Germany.
  29. Division of Pediatric Neurology, Department of Pediatric and Adolescent Medicine, University Medical Center, Göttingen, Germany.
  30. Institute for Auditory Neuroscience and InnerEarLab, University Medical Center, Göttingen, Germany.
  31. North East Thames Regional Genetics Service, Great Ormond Street Hospital for Children NHS Foundation Trust, London, WC1N 3JH, UK. [email protected].
  32. Genetic and Genomic Medicine Programme, UCL Great Ormond Street Institute of Child Health, London, WC1N 1EH, UK. [email protected].

PMID: 29435658 DOI: 10.1007/s00439-018-1870-7

Abstract

The following information was inadvertently omitted in the original publication.

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