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Whole exome sequencing identifies a mutation for a novel form of corneal intraepithelial dyskeratosis
  1. Vincent José Soler1,2,
  2. Khanh-Nhat Tran-Viet1,
  3. Stéphane D Galiacy2,
  4. Vachiranee Limviphuvadh3,
  5. Thomas Patrick Klemm4,
  6. Elizabeth St Germain1,
  7. Pierre R Fournié2,5,
  8. Céline Guillaud2,5,
  9. Sebastian Maurer-Stroh3,6,
  10. Felicia Hawthorne1,
  11. Cyrielle Suarez2,5,
  12. Bernadette Kantelip7,
  13. Natalie A Afshari8,
  14. Isabelle Creveaux9,
  15. Xiaoyan Luo1,
  16. Weihua Meng2,
  17. Patrick Calvas2,
  18. Myriam Cassagne2,5,
  19. Jean-Louis Arné5,
  20. Steven G Rozen4,
  21. François Malecaze2,5,
  22. Terri L Young1,8
  1. 1Duke Center for Human Genetics, Duke University Medical Center, Durham, North Carolina, USA
  2. 2EA-4555 Genetics of refractive disorders and developmental defects of the Eye, Centre de Physiopathologie de Toulouse Purpan, Toulouse III Paul-Sabatier University, Toulouse, France
  3. 3Bioinformatics Institute, Agency for Science Technology and Research, Singapore, Singapore
  4. 4Duke-National University of Singapore Graduate Medical School, Singapore, Singapore
  5. 5Ophthalmology Department, Purpan Hospital, Toulouse, France
  6. 6School of Biological Sciences, Nanyang Technological University, Singapore, Singapore
  7. 7Service d'Anatomie Pathologique, Centre Hospitalier Universitaire de Besançon, Besançon, France
  8. 8Department of Ophthalmology, Duke University Eye Center, Durham, North Carolina, USA
  9. 9Laboratoire de biochimie médicale et de biologie moléculaire, Faculté de médecine de Clermont-Ferrand, Clermont-Ferrand, France
  1. Correspondence to Dr Vincent José Soler, Ophthalmology Department, Pavillon Dieulafoy, Place Baylac, 31057 Toulouse Cedex 9, France; vincesoler{at}yahoo.fr

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