The first Mongolian cases of phenylketonuria in selective screening of inborn errors of metabolism

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Use this link to cite this item : https://ir.lib.shimane-u.ac.jp/53450

language	eng
Author	Purevsuren Jamiyan Chidlren's Hospital, National Center for Maternal and Child Health, Bayangol district, Ulaanbaatar 16060, Mongolia Bolormaa Baasandai Chidlren's Hospital, National Center for Maternal and Child Health, Bayangol district, Ulaanbaatar 16060, Mongolia Narantsetseg Chogdon Chidlren's Hospital, National Center for Maternal and Child Health, Bayangol district, Ulaanbaatar 16060, Mongolia Batsolongo Renchindorj Chidlren's Hospital, National Center for Maternal and Child Health, Bayangol district, Ulaanbaatar 16060, Mongolia Enkhchimeg Ochirbat Chidlren's Hospital, National Center for Maternal and Child Health, Bayangol district, Ulaanbaatar 16060, Mongolia Bayalag Munkhuu Chidlren's Hospital, National Center for Maternal and Child Health, Bayangol district, Ulaanbaatar 16060, Mongolia HASEGAWA, Yuki Shintaku Haruo Department of Pediatrics, Osaka City University Graduate School of Medicine, 1-4-3 Asahi-machi, Abeno-ku, Osaka 545-8585, Japan Yamaguchi, Seiji
Subject	Phenylketonuria; Inborn errors of metabolism; Mongolia; Screening
Journal Title	MOLECULAR GENETICS AND METABOLISM REPORTS
Volume	9
Start Page	71
End Page	74
ISSN（Online）	2214-4269
Published Date	2016-12
DOI	10.1016/j.ymgmr.2016.10.008
PubMed ID	27830119
Publisher	ELSEVIER
NII Type	Journal Article
OAI-PMH Set	Faculty of Medicine