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Prenylation defects in inherited retinal diseases

Authors

  • Susanne Roosing Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands Nijmegen Centre for Molecular Life Sciences, Radboud University Nijmegen, Nijmegen, The Netherlands PubMed articlesGoogle scholar articles
  • Rob W J Collin Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands Nijmegen Centre for Molecular Life Sciences, Radboud University Nijmegen, Nijmegen, The Netherlands PubMed articlesGoogle scholar articles
  • Anneke I den Hollander Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands Nijmegen Centre for Molecular Life Sciences, Radboud University Nijmegen, Nijmegen, The Netherlands Department of Ophthalmology, Radboud University Medical Center, Nijmegen, The Netherlands PubMed articlesGoogle scholar articles
  • Frans P M Cremers Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands Nijmegen Centre for Molecular Life Sciences, Radboud University Nijmegen, Nijmegen, The Netherlands PubMed articlesGoogle scholar articles
  • Anna M Siemiatkowska Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands PubMed articlesGoogle scholar articles
  1. Correspondence to Professor Frans P M Cremers, Department of Human Genetics, Radboud University Medical Center, PO Box 9101, 6500 HB, Nijmegen, The Netherlands; Frans.Cremers{at}radboudumc.nl
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Citation

Roosing S, Collin RWJ, den Hollander AI, et al
Prenylation defects in inherited retinal diseases

Publication history

  • Received October 23, 2013
  • Revised December 5, 2013
  • Accepted December 9, 2013
  • First published January 8, 2014.
Online issue publication 
February 14, 2014

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