A Missense Mutation inHK1Leads to Autosomal Dominant Retinitis Pigmentosa

Author:

Wang Feng1,Wang Yandong2,Zhang Bin1,Zhao Li3,Lyubasyuk Vera4,Wang Keqing1,Xu Mingchu1,Li Yumei1,Wu Frances4,Wen Cindy4,Bernstein Paul S.5,Lin Danni4,Zhu Susanna4,Wang Hui1,Zhang Kang6,Chen Rui7

Affiliation:

1. Human Genome Sequencing Center, Baylor College of Medicine, Houston, Texas, United States 2Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, United States

2. Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangzhou, China

3. Human Genome Sequencing Center, Baylor College of Medicine, Houston, Texas, United States 4Structural and Computational Biology and Molecular Biophysics Graduate Program, Baylor College of Medicine, Houston, Texas, United States

4. Shiley Eye Center and Institute for Genomic Medicine, University of California-San Diego, La Jolla, California, United States

5. Department of Ophthalmology and Visual Sciences, Moran Eye Center, University of Utah School of Medicine, Salt Lake City, Utah, United States

6. Shiley Eye Center and Institute for Genomic Medicine, University of California-San Diego, La Jolla, California, United States 7Veterans Administration Healthcare System, San Diego, California, United States

7. Human Genome Sequencing Center, Baylor College of Medicine, Houston, Texas, United States 2Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, United States 4Structural and Computational Biology and Molecular Biophysics

Publisher

Association for Research in Vision and Ophthalmology (ARVO)

Subject

General Medicine

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