Novel Null Mutations in theEYSGene Are a Frequent Cause of Autosomal Recessive Retinitis Pigmentosa in the Israeli Population

Author:

Bandah-Rozenfeld Dikla1,Littink Karin W.2,Ben-Yosef Tamar3,Strom Tim M.4,Chowers Itay1,Collin Rob W. J.5,den Hollander Anneke I.6,van den Born L. Ingeborgh7,Zonneveld Marijke N.8,Merin Saul1,Banin Eyal1,Cremers Frans P. M.9,Sharon Dror1

Affiliation:

1. From the Department of Ophthalmology, Hadassah-Hebrew University Medical Center, Jerusalem, Israel;

2. The Rotterdam Eye Hospital, Rotterdam, The Netherlands; the Departments of 3Human Genetics and

3. the Department of Genetics, The Rappaport Family Institute for Research in the Medical Sciences, Faculty of Medicine, Technion-Israel Institute of Technology, Haifa, Israel;

4. the Institute of Human Genetics, Helmholtz Zentrum Munchen, Neuherberg, Germany; and

5. the Departments of Human Genetics and 7Ophthalmology, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands; the 6Nijmegen Centre for Molecular Life Sciences, Radboud University Nijmegen, Nijmegen, The Netherlands.

6. Ophthalmology, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands; the 6Nijmegen Centre for Molecular Life Sciences, Radboud University Nijmegen, Nijmegen, The Netherlands.

7. The Rotterdam Eye Hospital, Rotterdam, The Netherlands;

8. the Departments of Human Genetics and

9. the Departments of Human Genetics and the 6Nijmegen Centre for Molecular Life Sciences, Radboud University Nijmegen, Nijmegen, The Netherlands.

Publisher

Association for Research in Vision and Ophthalmology (ARVO)

Subject

General Medicine

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