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Sukalo M, Tilsen F, Kayserili H, et al. DOCK6 Mutations Are Responsible for a Distinct Autosomal-Recessive Variant of Adams-Oliver Syndrome Associated with Brain and Eye Anomalies. Hum Mutat. 2015;36(11):1112doi: 10.1002/humu.22830.
Sukalo, M., Tilsen, F., Kayserili, H., Müller, D., Tüysüz, B., Ruddy, D. M., Wakeling, E., Ørstavik, K. H., Bramswig, N. C., Snape, K. M., Trembath, R., De Smedt, M., van der Aa, N., Skalej, M., Mundlos, S., Wuyts, W., Southgate, L., & Zenker, M. (2015). DOCK6 Mutations Are Responsible for a Distinct Autosomal-Recessive Variant of Adams-Oliver Syndrome Associated with Brain and Eye Anomalies. Human mutation, 36(11), 1112. https://doi.org/10.1002/humu.22830
Sukalo, Maja, et al. "DOCK6 Mutations Are Responsible for a Distinct Autosomal-Recessive Variant of Adams-Oliver Syndrome Associated with Brain and Eye Anomalies." Human mutation vol. 36,11 (2015): 1112. doi: https://doi.org/10.1002/humu.22830
Sukalo M, Tilsen F, Kayserili H, Müller D, Tüysüz B, Ruddy DM, Wakeling E, Ørstavik KH, Bramswig NC, Snape KM, Trembath R, De Smedt M, van der Aa N, Skalej M, Mundlos S, Wuyts W, Southgate L, Zenker M. DOCK6 Mutations Are Responsible for a Distinct Autosomal-Recessive Variant of Adams-Oliver Syndrome Associated with Brain and Eye Anomalies. Hum Mutat. 2015 Nov;36(11):1112. doi: 10.1002/humu.22830. Epub 2015 Aug 07. PMID: 26457590.
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Hum Mutat. 2015 Nov;36(11):1112. doi: 10.1002/humu.22830. Epub 2015 Aug 07.

DOCK6 Mutations Are Responsible for a Distinct Autosomal-Recessive Variant of Adams-Oliver Syndrome Associated with Brain and Eye Anomalies.

Human mutation

Maja Sukalo, Felix Tilsen, Hülya Kayserili, Dietmar Müller, Beyhan Tüysüz, Deborah M Ruddy, Emma Wakeling, Karen Helene Ørstavik, Nuria C Bramswig, Katie M Snape, Richard Trembath, Maryse De Smedt, Nathalie van der Aa, Martin Skalej, Stefan Mundlos, Wim Wuyts, Laura Southgate, Martin Zenker

Affiliations

  1. Institute of Human Genetics, University Hospital Magdeburg, Magdeburg, Germany.
  2. Medical Genetics Department, Istanbul Medical Faculty, Istanbul, Turkey.
  3. Institut für Medizinische Genetik, Klinikum Chemnitz, Chemnitz, Germany.
  4. Department of Pediatric Genetics, Istanbul University, Istanbul, Turkey.
  5. Department of Clinical Genetics, Guy's Hospital, London, UK.
  6. North West Thames Regional Genetics Service, North West London Hospitals NHS Trust, Harrow, UK.
  7. Department of Medical Genetics, Oslo University Hospital, Oslo, Norway.
  8. Institut für Humangenetik, Universitätsklinikum Essen, Universität Duisburg-Essen, Essen, Germany.
  9. Department of Clinical Genetics, St George's Healthcare NHS Trust, London, UK.
  10. Barts and The London School of Medicine and Dentistry, Queen Mary University of London, London, UK.
  11. Department of Medical Genetics, Leuven University Hospital, Leuven, Belgium.
  12. Department of Medical Genetics, Antwerp University Hospital, Antwerp, Belgium.
  13. Institute of Neuroradiology, Otto von Guericke University Magdeburg, Magdeburg, Germany.
  14. Institute for Medical and Human Genetics Charité, Universitätsmedizin Berlin and Max Planck Institute for Molecular Genetics Berlin, Berlin, Germany.
  15. Department of Medical Genetics, University of Antwerp, Antwerp, Belgium.
  16. Division of Genetics and Molecular Medicine, King's College London, London, UK.

PMID: 26457590 DOI: 10.1002/humu.22830

Abstract

The original article to which this Erratum refers was published in Human Mutation 36(6):593–598(DOI:10.1002/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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