Human Genetics of Truncus Arteriosus.
| Autor: | Yamagishi H; Division of Pediatric Cardiology, Department of Pediatrics, Keio University School of Medicine, Tokyo, Japan. hyamag@keio.jp. |
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| Jazyk: | angličtina |
| Zdroj: | Advances in experimental medicine and biology [Adv Exp Med Biol] 2024; Vol. 1441, pp. 841-852. |
| DOI: | 10.1007/978-3-031-44087-8_51 |
| Abstrakt: | Integrated human genetics and molecular/developmental biology studies have revealed that truncus arteriosus is highly associated with 22q11.2 deletion syndrome. Other congenital malformation syndromes and variants in genes encoding TBX, GATA, and NKX transcription factors and some signaling proteins have also been reported as its etiology. (© 2024. The Author(s), under exclusive license to Springer Nature Switzerland AG.) |
| Databáze: | MEDLINE |
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