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J-GLOBAL ID：201902210129094242   Reference number：19S1387849

MPV17 mutations in patients with hepatocerebral mitochondrial DNA depletion syndrome

Author (12)： Kim, Joonil (Department of Pediatrics, Asan Medical Center Children's Hospital, University of Ulsan College of Medicine) ,  Kang, Eungu (Department of Pediatrics, Asan Medical Center Children's Hospital, University of Ulsan College of Medicine) ,  Kim, Yoonmyung (Department of Pediatrics, Asan Medical Center Children's Hospital, University of Ulsan College of Medicine) ,  Lee, Beom Hee (Department of Pediatrics, Asan Medical Center Children's Hospital, University of Ulsan College of Medicine) ,  Lee, Beom Hee (Medical Genetics Center, Asan Medical Center Children's Hospital, University of Ulsan College of Medicine) ,  Kim, Kyung Mo (Department of Pediatrics, Asan Medical Center Children's Hospital, University of Ulsan College of Medicine) ,  Yoo, Han-Wook (Department of Pediatrics, Asan Medical Center Children's Hospital, University of Ulsan College of Medicine) ,  Yoo, Han-Wook (Medical Genetics Center, Asan Medical Center Children's Hospital, University of Ulsan College of Medicine) ,  Kim, Jae-Min (Medical Genetics Center, Asan Medical Center Children's Hospital, University of Ulsan College of Medicine) ,  Kim, Gu-Hwan (Medical Genetics Center, Asan Medical Center Children's Hospital, University of Ulsan College of Medicine) ,  Choi, In Hee (Medical Genetics Center, Asan Medical Center Children's Hospital, University of Ulsan College of Medicine) ,  Murayama, Kei (Department of Metabolism, Chiba Children's Hospital)
Material： Molecular Genetics and Metabolism Reports
Volume： 8  Page： 74-76  Publication year： 2016 
JST Material Number： SCOPUS  ISSN： 2214-4269 
Country of issue： United States (USA)  Language： English (EN)

Terms in the title (1)： DNA