講演情報
[II-JCKAP5-1-4]The TMEM260 c.1617del variant is identified as the most frequent single gene determinant for persistent truncus arteriosus in Japanese population
○Tadashi Inoue1,2, Ryuta Takase2, Keiko Uchida1,3, Kazuki Kodo1,4, Kenji Suda2, Yoriko Watanabe2,5, Masaya Kunimatsu1,6, Reina Ishizaki1, Hiroyuki Akagawa7, Hiroyuki Yamagishi1,8 (1.Department of Pediatrics, Keio University School of Medicine, Tokyo, 2.Department of Pediatrics and Child Health, Kurume University School of Medicine, Fukuoka, 3.Department of Physiology, Tokyo Medical University, Tokyo, 4.Department of Pediatrics, Tokyo Metropolitan Otsuka Hospital, Tokyo, 5.Research Institute of Medical Mass Spectrometry, Kurume University School of Medicine, Fukuoka, 6.Department of Pediatrics, Chiba University Graduate School of Medicine, Chiba, 7.Institute for Comprehensive Medical Sciences, Tokyo Women's Medical University, Tokyo, 8.Tokyo Metropolitan Children's Medical Center, Tokyo)
キーワード:
outflow tract defects、exome sequencing、heart development
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パスワードは「2024年 ニュースレター No.2(冊子のみ)、会員への配信メール」に記載されています。
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