Review Article
Diagnosis and treatment of mitochondrial diabetes associated with m.3243A>G mutation
Shang Lijing, Peng Huifang, Zhao Qian, Ma Yujin, Jiang Hongwei
Published 2021-05-27
Cite as Chin J Diabetes Mellitus, 2021, 13(5): 509-512. DOI: 10.3760/cma.j.cn115791-20200808-00492
Contributor Information
Shang Lijing
Department of Endocrinology and Metabolism, the First Affiliated Hospital, and College of Clinical Medicine of Henan University of Science and Technology, Luoyang City Clinical Research for Endocrinology and Metabolism, Medical Key Laboratory of Hereditary Rare Diseases of Henan, Luoyang 471003, China
Peng Huifang
Department of Endocrinology and Metabolism, the First Affiliated Hospital, and College of Clinical Medicine of Henan University of Science and Technology, Luoyang City Clinical Research for Endocrinology and Metabolism, Medical Key Laboratory of Hereditary Rare Diseases of Henan, Luoyang 471003, China
Zhao Qian
Department of Endocrinology and Metabolism, the First Affiliated Hospital, and College of Clinical Medicine of Henan University of Science and Technology, Luoyang City Clinical Research for Endocrinology and Metabolism, Medical Key Laboratory of Hereditary Rare Diseases of Henan, Luoyang 471003, China
Ma Yujin
Department of Endocrinology and Metabolism, the First Affiliated Hospital, and College of Clinical Medicine of Henan University of Science and Technology, Luoyang City Clinical Research for Endocrinology and Metabolism, Medical Key Laboratory of Hereditary Rare Diseases of Henan, Luoyang 471003, China
Jiang Hongwei
Department of Endocrinology and Metabolism, the First Affiliated Hospital, and College of Clinical Medicine of Henan University of Science and Technology, Luoyang City Clinical Research for Endocrinology and Metabolism, Medical Key Laboratory of Hereditary Rare Diseases of Henan, Luoyang 471003, China
