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KCNA4 deficiency leads to a syndrome of abnormal striatum, congenital cataract and intellectual disability
  1. Namik Kaya1,
  2. Maysoon Alsagob1,
  3. Maria Cristina D'Adamo2,
  4. Albandary Al-Bakheet1,
  5. Sonia Hasan2,
  6. Maria Muccioli3,
  7. Faten B Almutairi1,
  8. Rawan Almass1,
  9. Mazhor Aldosary1,
  10. Dorota Monies1,
  11. Osama M Mustafa1,4,
  12. Banan Alyounes1,
  13. Rosan Kenana1,
  14. Jawaher Al-Zahrani1,
  15. Eva Naim1,
  16. Faisal S Binhumaid1,
  17. Alya Qari5,
  18. Fatema Almutairi1,
  19. Brian Meyer1,
  20. Timothy F Plageman3,
  21. Mauro Pessia2,6,
  22. Dilek Colak7,
  23. Mohammed Al-Owain3,4
  1. 1Department of Genetics, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia
  2. 2Section of Physiology and Biochemistry, Department of Experimental Medicine, University of Perugia School of Medicine, Perugia, Italy
  3. 3College of Optometry, The Ohio State University, Columbus, Ohio, USA
  4. 4College of Medicine, Alfaisal University, Riyadh, Saudi Arabia
  5. 5Department of Medical Genetics, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia
  6. 6Department of Physiology & Biochemistry Faculty of Medicine & Surgery, University of Malta, Msida, Malta
  7. 7Department of Biostatistics, Epidemiology and Scientific Computing, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia
  1. Correspondence to Dr Namik Kaya, Department of Genetics, King Faisal Specialist Hospital and Research Centre, MBC:03, P.O. Box 3354, Riyadh 11211, Saudi Arabia; nkaya{at}kfshrc.edu.sa Dr Mohammed Al-Owain Department of Medical Genetics, King Faisal Specialist Hospital and Research Centre, P.O. Box 3354, Riyadh 11211, Saudi Arabia; alowain{at}kfshrc.edu.sa

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