Mutations in theUBIAD1Gene on Chromosome Short Arm 1, Region 36, Cause Schnyder Crystalline Corneal Dystrophy

Author:

Weiss Jayne S.1,Kruth Howard S.2,Kuivaniemi Helena3,Tromp Gerard4,White Peter S.5,Winters R. Scott5,Lisch Walter6,Henn Wolfram7,Denninger Elke8,Krause Matthias8,Wasson Paul9,Ebenezer Neil10,Mahurkar Sunil11,Nickerson Michael L.11

Affiliation:

1. From the Kresge Eye Institute, the2Departments of Ophthalmology and

2. Section of Experimental Atherosclerosis, National Institutes of Health, Bethesda, Maryland;

3. Surgery, and the4Center for Molecular Medicine and Genetics, Wayne State University School of Medicine, Detroit, Michigan; the

4. Center for Molecular Medicine and Genetics, Wayne State University School of Medicine, Detroit, Michigan; the

5. Children’s Hospital of Philadelphia, Philadelphia, Pennsylvania; the

6. Department of Ophthalmology, Klinikum Hanau, Hanau, Germany; the

7. Departments of Human Genetics and

8. Ophthalmology, Saarland University, Homburg-Saar, Germany; the

9. Massachusetts Eye and Ear Infirmary, Boston, Massachusetts; the

10. Department of Molecular Genetics, The Institute of Ophthalmology, University College London, London, United Kingdom; and

11. Transgenomic, Gaithersburg, Maryland.

Publisher

Association for Research in Vision and Ophthalmology (ARVO)

Subject

General Medicine

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