# 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

**Authors:** Hisao Yaoita, Eiichiro Kawai, Jun Takayama, Shinya Iwasawa, Naoya Saijo, Masayuki Abiko, Kouta Suzuki, Masato Kimura, Akira Ozawa, Gen Tamiya, Shigeo Kure, Atsuo Kikuchi

PMC · DOI: 10.1038/s10038-024-01245-6 · 2024-03-29

## Full-text entities

- **Genes:** TMEM260 (transmembrane protein 260) [NCBI Gene 54916] {aka C14orf101, SHDRA}
- **Diseases:** 22q11.2 deletion syndrome (MESH:D004062), truncus arteriosus (MESH:D014339)
- **Mutations:** c.1617del

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Source: https://tomesphere.com/paper/PMC11043029