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DOCK6 Mutations Are Responsible for a Distinct Autosomal-Recessive Variant of Adams-Oliver Syndrome Associated with Brain and Eye Anomalies.
Sukalo, Maja; Tilsen, Felix; Kayserili, Hülya; Müller, Dietmar; Tüysüz, Beyhan; Ruddy, Deborah M; Wakeling, Emma; Ørstavik, Karen Helene; Bramswig, Nuria C; Snape, Katie M; Trembath, Richard; De Smedt, Maryse; van der Aa, Nathalie; Skalej, Martin; Mundlos, Stefan; Wuyts, Wim; Southgate, Laura; Zenker, Martin.
Afiliación
  • Sukalo M; Institute of Human Genetics, University Hospital Magdeburg, Magdeburg, Germany.
  • Tilsen F; Institute of Human Genetics, University Hospital Magdeburg, Magdeburg, Germany.
  • Kayserili H; Medical Genetics Department, Istanbul Medical Faculty, Istanbul, Turkey.
  • Müller D; Institut für Medizinische Genetik, Klinikum Chemnitz, Chemnitz, Germany.
  • Tüysüz B; Department of Pediatric Genetics, Istanbul University, Istanbul, Turkey.
  • Ruddy DM; Department of Clinical Genetics, Guy's Hospital, London, UK.
  • Wakeling E; North West Thames Regional Genetics Service, North West London Hospitals NHS Trust, Harrow, UK.
  • Ørstavik KH; Department of Medical Genetics, Oslo University Hospital, Oslo, Norway.
  • Bramswig NC; Institut für Humangenetik, Universitätsklinikum Essen, Universität Duisburg-Essen, Essen, Germany.
  • Snape KM; Department of Clinical Genetics, St George's Healthcare NHS Trust, London, UK.
  • Trembath R; Department of Clinical Genetics, Guy's Hospital, London, UK.
  • De Smedt M; Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, UK.
  • van der Aa N; Department of Medical Genetics, Leuven University Hospital, Leuven, Belgium.
  • Skalej M; Department of Medical Genetics, Antwerp University Hospital, Antwerp, Belgium.
  • Mundlos S; Institute of Neuroradiology, Otto von Guericke University Magdeburg, Magdeburg, Germany.
  • Wuyts W; Institute for Medical and Human Genetics Charité, Universitätsmedizin Berlin and Max Planck Institute for Molecular Genetics Berlin, Berlin, Germany.
  • Southgate L; Department of Medical Genetics, Antwerp University Hospital, Antwerp, Belgium.
  • Zenker M; Department of Medical Genetics, University of Antwerp, Antwerp, Belgium.
Hum Mutat ; 36(11): 1112, 2015 Nov.
Article en En | MEDLINE | ID: mdl-26457590
ABSTRACT
The original article to which this Erratum refers was published in Human Mutation 36(6)593­598(DOI10.1002/humu22795).The authors realized that a co-author, Nuria C. Bramswig, was left off of the title page of this article at the time of submission. This erratum serves to correct this error by including Dr. Bramswig and Dr. Bramswig's institution in the title page information.The authors regret the error.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Risk_factors_studies Idioma: En Revista: Hum Mutat Asunto de la revista: GENETICA MEDICA Año: 2015 Tipo del documento: Article País de afiliación: Alemania
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Risk_factors_studies Idioma: En Revista: Hum Mutat Asunto de la revista: GENETICA MEDICA Año: 2015 Tipo del documento: Article País de afiliación: Alemania