Identification of TBX2 and TBX3 variants in patients with conotruncal heart defects by target sequencing
Abstract Background Conotruncal heart defects (CTDs) are heterogeneous congenital heart malformations that result from outflow tract dysplasia; however, the genetic determinants underlying CTDs remain unclear. Increasing evidence demonstrates that dysfunctional TBX2 and TBX3 result in outflow tract...
Αποθηκεύτηκε σε:
| Κύριοι συγγραφείς: | , , , , , , , |
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| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
BMC
2018-09-01
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| Σειρά: | Human Genomics |
| Θέματα: | |
| Διαθέσιμο Online: | http://link.springer.com/article/10.1186/s40246-018-0176-0 |
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