Correction: The c.1617del variant of TMEM260 is identified as the most frequent single gene determinant for Japanese patients with a specific type of congenital heart disease

J Hum Genet. 2024 May;69(5):223. doi: 10.1038/s10038-024-01238-5.

Tadashi Inoue^{1

2}, Ryuta Takase², Keiko Uchida^{3

4}, Kazuki Kodo¹, Kenji Suda², Yoriko Watanabe^{2

5}, Koh-Ichiro Yoshiura⁶, Masaya Kunimatsu^{1

7}, Reina Ishizaki¹, Kenko Azuma⁸, Kei Inai⁹, Jun Muneuchi¹⁰, Yoshiyuki Furutani⁹, Hiroyuki Akagawa⁸, Hiroyuki Yamagishi^{1

11}

¹ Department of Pediatrics, Keio University School of Medicine, Tokyo, Japan.
² Department of Pediatrics and Child Health, Kurume University School of Medicine, Fukuoka, Japan.
³ Department of Pediatrics, Keio University School of Medicine, Tokyo, Japan. keiuchid@keio.jp.
⁴ Keio University Health Center, Tokyo, Japan. keiuchid@keio.jp.
⁵ Research Institute of Medical Mass Spectrometry, Kurume University School of Medicine, Fukuoka, Japan.
⁶ Department of Human Genetics, Division of Advanced Preventive Medical Sciences, Leading Medical Research Core Unit, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
⁷ Department of Pediatrics, Chiba University Graduate School of Medicine, Chiba, Japan.
⁸ Institute for Comprehensive Medical Sciences, Tokyo Women's Medical University, Tokyo, Japan.
⁹ Department of Pediatric Cardiology and Adult Congenital Cardiology, Tokyo Women's Medical University, Tokyo, Japan.
¹⁰ Department of Pediatrics, Kyushu Hospital, Japan Community Healthcare Organization, Kitakyushu, Japan.
¹¹ Center for Preventive Medicine, Keio University School of Medicine, Tokyo, Japan.

No abstract available

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