X-linked Retinitis Pigmentosa:RPGRMutations in Most Families with Definite X Linkage and Clustering of Mutations in a Short Sequence Stretch of Exon ORF15

Author:

Bader Ingrid1,Brandau Oliver2,Achatz Helene2,Apfelstedt-Sylla Eckart3,Hergersberg Martin4,Lorenz Birgit5,Wissinger Bernd6,Wittwer Ba¨rbel7,Rudolph Gu¨nther8,Meindl Alfons2,Meitinger Thomas9

Affiliation:

1. From the Institute of Human Genetics, National Research Center for Environment and Health (GSF), Neuherberg, Germany; the

2. Department of Medical Genetics at the University of Munich, Munich, Germany; the

3. University Eye Hospital Tu¨bingen, Tu¨bingen, Germany; the

4. Center for Laboratory Medicine, Cantonal Hospital Aarau, Aarau, Switzerland; the

5. Department of Paediatric Ophthalmology, Strabismology, and Ophthalmogenetics, Regensburg, Germany; the

6. Molecular Genetics Laboratory, University Eye Hospital Tu¨bingen, Tu¨bingen, Germany; the

7. Institute of Human Genetics, Mu¨nster, Germany; the

8. University Eye Clinic, Munich, Germany; and

9. From the Institute of Human Genetics, National Research Center for Environment and Health (GSF), Neuherberg, Germany; the11GSF-Clinical Cooperation Group Ophthalmogenetics, Neuherberg, Germany.

Publisher

Association for Research in Vision and Ophthalmology (ARVO)

Subject

General Medicine

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