טוען...
A novel TBX5 mutation predisposes to familial cardiac septal defects and atrial fibrillation as well as bicuspid aortic valve
TBX5 has been linked to Holt-Oram syndrome, with congenital heart defect (CHD) and atrial fibrillation (AF) being two major cardiac phenotypes. However, the prevalence of a TBX5 variation in patients with CHD and AF remains obscure. In this research, by sequencing analysis of TBX5 in 178 index patie...
שמור ב:
| הוצא לאור ב: | Genet Mol Biol |
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| Main Authors: | , , , , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
Sociedade Brasileira de Genética
2020
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7783509/ https://ncbi.nlm.nih.gov/pubmed/33306779 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1590/1678-4685-GMB-2020-0142 |
| תגים: |
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