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.
作者信息
Yaoita Hisao, Kawai Eiichiro, Takayama Jun, Iwasawa Shinya, Saijo Naoya, Abiko Masayuki, Suzuki Kouta, Kimura Masato, Ozawa Akira, Tamiya Gen, Kure Shigeo, Kikuchi Atsuo
机构信息
Department of Pediatrics, Tohoku University Graduate School of Medicine, Sendai, Japan.
Department of Pediatric Cardiology, Miyagi Children's Hospital, Sendai, Japan.
出版信息
J Hum Genet. 2024 May;69(5):185. doi: 10.1038/s10038-024-01245-6.
Abstract
摘要
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1
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.更正：法洛四联症的遗传病因（不包括22q11.2缺失综合征）以及在日本人群中鉴定出TMEM260中一种常见变异c.1617del。
J Hum Genet. 2024 May;69(5):185. doi: 10.1038/s10038-024-01245-6.
2
Genetic etiology of truncus arteriosus excluding 22q11.2 deletion syndrome and identification of c.1617del, a prevalent variant in TMEM260, in the Japanese population.不包括22q11.2缺失综合征的动脉干的遗传病因，并在日本人群中鉴定出TMEM260中一种常见变异c.1617del。
J Hum Genet. 2024 May;69(5):177-183. doi: 10.1038/s10038-024-01223-y. Epub 2024 Feb 13.
3
A Prevalent TMEM260 Deletion Causes Conotruncal Heart Defects, Including Truncus Arteriosus.一种常见的TMEM260缺失会导致圆锥动脉干心脏缺陷，包括永存动脉干。
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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.TMEM260基因的c.1617del变异被确定为患有特定类型先天性心脏病的日本患者最常见的单基因决定因素。
J Hum Genet. 2024 May;69(5):215-222. doi: 10.1038/s10038-024-01225-w. Epub 2024 Feb 26.
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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.更正：TMEM260基因的c.1617del变异被确定为特定类型先天性心脏病日本患者最常见的单基因决定因素。
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Front Med (Lausanne). 2023 May 9;10:1157042. doi: 10.3389/fmed.2023.1157042. eCollection 2023.
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