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J-GLOBAL ID：201902210192051286   Reference number：19S1401517

Significance of ACADM mutations identified through newborn screening of MCAD deficiency in Japan

Author (15)： Hara, Keiichi (Department of Pediatrics, National Hospital Organization Kure Medical Center) ,  Hara, Keiichi (Department of Pediatrics, Hiroshima University Graduate School of Biomedical and Health Sciences) ,  Tajima, Go (Department of Pediatrics, Hiroshima University Graduate School of Biomedical and Health Sciences) ,  Okada, Satoshi (Department of Pediatrics, Hiroshima University Graduate School of Biomedical and Health Sciences) ,  Tsumura, Miyuki (Department of Pediatrics, Hiroshima University Graduate School of Biomedical and Health Sciences) ,  Kagawa, Reiko (Department of Pediatrics, Hiroshima University Graduate School of Biomedical and Health Sciences) ,  Kobayashi, Masao (Department of Pediatrics, Hiroshima University Graduate School of Biomedical and Health Sciences) ,  Shirao, Kenichiro (Shirao Clinic of Pediatrics and Pediatric Allergy, Department of Pediatrics) ,  Ohno, Yoshinori (Department of Stem Cell Biology, Research Institute for Radiation Biology and Medicine, Hiroshima University) ,  Takihara, Yoshihiro (Department of Stem Cell Biology, Research Institute for Radiation Biology and Medicine, Hiroshima University) ,  Yasunaga, Shin'ichiro (Department of Biochemistry, Faculty of Medicine, Fukuoka University) ,  Ohtsubo, Motoaki (Department of Food and Nutrition, Beppu University) ,  Hata, Ikue (Department of Pediatrics, Faculty of Medical Sciences, University of Fukui) ,  Sakura, Nobuo (Nursing House for Severe Motor and Intellectual Disabilities SUZUGAMINE) ,  Shigematsu, Yosuke (Department of Health Science, Faculty of Medical Sciences, University of Fukui)
Material： Molecular Genetics and Metabolism
Volume： 118  Issue： 1  Page： 9-14  Publication year： 2016 
JST Material Number： SCOPUS  ISSN： 1096-7192  CODEN： MGMEF 
Country of issue： United States (USA)  Language： English (EN)