The CAPOS mutation in ATP1A3 alters Na/K-ATPase function and results in auditory neuropathy which has implications for management (vol 137, pg 111, 2018)

Tranebjaerg, Lisbeth (författare)

Department of Otorhinolaryngology, Head and Neck Surgery and Audiology, Rigshospitalet/Bispebjerg, Copenhagen, Denmark; Department of Clinical Genetics, The Kennedy Center, Copenhagen University Hospital, Copenhagen, Denmark; Institute of Clinical Medicine, University of Copenhagen, Copenhagen, Denmark

Strenzke, Nicola (författare)

Auditory Systems Physiology Group, InnerEarLab, Department of Otolaryngology, University Medical Center, Göttingen, Germany

Lindholm, Sture (författare)

ENT-Department, County Hospital Kalmar, Kalmar, Sweden

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Rendtorff, Nanna D. (författare)

Department of Clinical Genetics, The Kennedy Center, Copenhagen University Hospital, Copenhagen, Denmark

Poulsen, Hanne (författare)

Institute of Biomedicine, University of Aarhus, Aarhus, Denmark

Khandelia, Himanshu (författare)

MEMPHYS-Center for Biomembrane Physics, University of Southern Denmark, Odense, Denmark

Kopec, Wojciech (författare)

MEMPHYS-Center for Biomembrane Physics, University of Southern Denmark, Odense, Denmark; Computational Biomolecular Dynamics Group, Max Planck Institute for Biophysical Chemistry, Göttingen, Germany

Lyngbye, Troels J. Brunnich (författare)

Pediatric Department, Aarhus University Hospital, Aarhus, Denmark

Hamel, Christian (författare)

Maladies Sensorielles Genetiques, Centre Hospitalier Régional Universitaire (CHRU), Montpellier, France; Institute for Neurosciences of Montpellier (INSERM U1051), Montpellier, France; Universite Montpellier, Montpellier, France

Delettre, Cecile (författare)

Institute for Neurosciences of Montpellier (INSERM U1051), Montpellier, France; Universite Montpellier, Montpellier, France

Bocquet, Beatrice (författare)

Maladies Sensorielles Genetiques, Centre Hospitalier Régional Universitaire (CHRU), Montpellier, France; Institute for Neurosciences of Montpellier (INSERM U1051), Montpellier, France; Universite Montpellier, Montpellier, France

Bille, Michael (författare)

Department of Otorhinolaryngology, Head and Neck Surgery and Audiology, Rigshospitalet Gentofte Hospital, Hellerup, Denmark

Owen, Hanne H. (författare)

Department of Audiology, Aarhus University Hospital, Aarhus, Denmark

Bek, Toke (författare)

Department of Ophthalmology, Aarhus University Hospital, Aarhus, Denmark

Jensen, Hanne (författare)

Eye Department, The Kennedy Centre, Glostrup Hospital Rigshospitalet, Glostrup, Denmark

Østergaard, Karen (författare)

Department of Neurology, University Hospital, Aarhus, Denmark; University of Aarhus, Aarhus, Denmark

Möller, Claes, 1950- (författare)

Örebro universitet,Institutionen för hälsovetenskaper,Audiological Research Centre

Luxon, Linda (författare)

Department of Neurotology, National Hospital for Neurology, Queen Square, London, UK

Carr, Lucinda (författare)

Department of Neurology, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK

Wilson, Louise (författare)

North East Thames Regional Genetics Service, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK

Rajput, Kaukab (författare)

Cochlear Implant Department, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK

Sirimanna, Tony (författare)

Department of Audiovestibular Medicine, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK

Harrop-Griffiths, Katherine (författare)

Nuffield Hearing and Speech Centre, Royal National Throat Nose and Ear Hospital, London, UK

Rahman, Shamima (författare)

Genetic and Genomic Medicine Programme, UCL Great Ormond Street Institute of Child Health, London, UK

Vona, Barbara (författare)

Institute of Human Genetics, Julius Maximilians University, Würzburg, Germany

Doll, Julia (författare)

Institute of Human Genetics, Julius Maximilians University, Würzburg, Germany

Haaf, Thomas (författare)

Institute of Human Genetics, Julius Maximilians University, Würzburg, Germany

Bartsch, Oliver (författare)

Institute of Human Genetics, University Medical Centre, Johannes Gutenberg University Mainz, Mainz, Germany

Rosewich, Hendrik (författare)

Division of Pediatric Neurology, Department of Pediatric and Adolescent Medicine, University Medical Center, Göttingen, Germany

Moser, Tobias (författare)

Institute for Auditory Neuroscience and InnerEarLab, University Medical Center, Göttingen, Germany

Bitner-Glindzicz, Maria (författare)

North East Thames Regional Genetics Service, Great Ormond Street Hospital for Children NHS Foundation Trust, London, UK; Genetic and Genomic Medicine Programme, UCL Great Ormond Street Institute of Child Health, London, UK

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 (creator_code:org_t)

2018-02-12

2018

Engelska.

Ingår i: Human Genetics. - : Springer. - 0340-6717 .- 1432-1203. ; 137:3, s. 279-280

Relaterad länk:

https://link.springe...

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https://urn.kb.se/re...

https://doi.org/10.1...

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• Tidskriftsartikel (refereegranskat)