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Association of NKX2‐5, GATA4, and TBX5 polymorphisms with congenital heart disease in Egyptian children
BACKGROUND: Several genes encoding transcription factors are known to be the primary cause of congenital heart disease. NKX2‐5 and GATA4 were the first congenital heart disease–causing genes identified by linkage analysis. This study designed to study the association of five single–nucleotide varian...
Gorde:
| Argitaratua izan da: | Mol Genet Genomic Med |
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| Egile Nagusiak: | , , , , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
John Wiley and Sons Inc.
2019
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6503026/ https://ncbi.nlm.nih.gov/pubmed/30834692 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.612 |
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