Depletion of Uric Acid Due to SLC22A12 (URAT1) Loss-of-Function Mutation Causes Endothelial Dysfunction in Hypouricemia

Author:

Sugihara Shinobu1,Hisatome Ichiro2,Kuwabara Masanari3,Niwa Koichiro3,Maharani Nani2,Kato Masahiko1,Ogino Kazuhide4,Hamada Toshihiro5,Ninomiya Haruaki6,Higashi Yukihito7,Ichida Kimiyoshi8,Yamamoto Kazuhiro1

Affiliation:

1. Division of Cardiovascular Medicine, Department of Molecular Medicine and Therapeutics Faculty of Medicine, Tottori University

2. Department of Genetic Medicine and Regenerative Therapeutics, Institute of Regenerative Medicine and Biofunction, Tottori University Graduate School of Medical Science

3. Department of Cardiology, St. Luke’s International Hospital

4. Department of Clinical Laboratory, Tottori University Hospital

5. Department of Regional Medicine, Tottori University Faculty of Medicine

6. Department of Biological Regulation, Tottori University Faculty of Medicine

7. Department of Regeneration and Medicine, Research Center for Radiation Genome Medicine, Research Institute for Radiation Biology and Medicine Hiroshima University

8. Department of Pathophysiology, Tokyo University of Pharmacy and Life science

Publisher

Japanese Circulation Society

Subject

Cardiology and Cardiovascular Medicine,General Medicine

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