Correction: Genetic etiology of truncus arteriosus excluding 22q11.2 deletion syndrome and identification of c.1617del, a prevalent variant in TMEM260, in the Japanese population

J Hum Genet. 2024 May;69(5):185. doi: 10.1038/s10038-024-01245-6.

Hisao Yaoita^#¹, Eiichiro Kawai^#², Jun Takayama^#^{3

4

5

6}, Shinya Iwasawa⁷, Naoya Saijo⁷, Masayuki Abiko⁸, Kouta Suzuki⁸, Masato Kimura², Akira Ozawa², Gen Tamiya^{3

4

5

6}, Shigeo Kure^{7

6

9}, Atsuo Kikuchi^{10

11}

¹ Department of Pediatrics, Tohoku University Graduate School of Medicine, Sendai, Japan. yaoita.hisao.r4@dc.tohoku.ac.jp.
² Department of Pediatric Cardiology, Miyagi Children's Hospital, Sendai, Japan.
³ Department of AI and Innovative Medicine, Tohoku University Graduate School of Medicine, Sendai, Japan.
⁴ Tohoku Medical Megabank organization, Tohoku University, Sendai, Japan.
⁵ Statistical Genetics Team, RIKEN Center for Advanced Intelligence Project, Tokyo, Japan.
⁶ Department of Rare Disease Genomics, Tohoku University Graduate School of Medicine, Sendai, Japan.
⁷ Department of Pediatrics, Tohoku University Graduate School of Medicine, Sendai, Japan.
⁸ Department of Pediatrics, Yamagata University Graduate School of Medicine, Yamagata, Japan.
⁹ Miyagi Children's Hospital, Sendai, Japan.
¹⁰ Department of Pediatrics, Tohoku University Graduate School of Medicine, Sendai, Japan. atsuo.kikuchi.d4@dc.tohoku.ac.jp.
¹¹ Department of Rare Disease Genomics, Tohoku University Graduate School of Medicine, Sendai, Japan. atsuo.kikuchi.d4@dc.tohoku.ac.jp.

^# Contributed equally.

No abstract available

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