language |
eng
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Author |
Musha, Ikuma
Department of Pediatrics, Faculty of Medicine, Saitama Medical University, 38 Morohongo, Moroyama-cho, Saitama 350-0495, Japan
Awano, Hiroyuki
Department of Pediatrics, Kobe University Graduate School of Medicine, 7-5-1 Kusunoki-cho, Chuo-ku, Kobe 650-0017, Japan
Arao, Masato
Department of Pediatrics, Faculty of Medicine, Saitama Medical University, 38 Morohongo, Moroyama-cho, Saitama 350-0495, Japan
Kikuchi, Toru
Department of Pediatrics, Faculty of Medicine, Saitama Medical University, 38 Morohongo, Moroyama-cho, Saitama 350-0495, Japan
Ohtake, Akira
Department of Pediatrics, Faculty of Medicine, Saitama Medical University, 38 Morohongo, Moroyama-cho, Saitama 350-0495, Japan
Yamaguchi, Seiji
Iijima, Kazumoto
Department of Pediatrics, Kobe University Graduate School of Medicine, 7-5-1 Kusunoki-cho, Chuo-ku, Kobe 650-0017, Japan
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Subject | Carnitine palmitoyltransferase II deficiency; Metabolic decompensation; Fatty acid oxidation disorders; Sudden unexpected death in infancy (SUDI)
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Journal Title |
MOLECULAR GENETICS AND METABOLISM REPORTS
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Volume | 24
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ISSN(Online) | 2214-4269
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Published Date | 2020-09
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DOI | |
PubMed ID | |
Publisher | ELSEVIER
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NII Type |
Journal Article
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OAI-PMH Set |
Faculty of Medicine
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Remark | We thank Ms. M. Furui, K. Konada, H. Kajitani, and T. Esumi (Department of Pediatrics, Shimane University) for their technical assistance. We also thank Dr. Go Tajima (Division of Neonatal Screening, Research Institute, National Center for Child Health and Development) for assisting with CPTII enzyme assay. This research was partially supported by Grant Number 15K09593 (Chief Investigator: Seiji Yamaguchi) and 19K17298 (Chief Investigator: Ryosuke Bo) from the Ministry of Health, Labor and Welfare of Japan.
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