Lataa...
Genetic abnormalities in FOXP1 are associated with congenital heart defects
The etiology for the majority of congenital heart defects (CHD) is unknown. We identified a patient with unbalanced atrioventricular septal defect (AVSD) and hypoplastic left ventricle who harbored an ~0.3Mb monoallelic deletion on chromosome 3p14.1. The deletion encompassed the first 4 exons of FOX...
Tallennettuna:
| Julkaisussa: | Hum Mutat |
|---|---|
| Päätekijät: | , , , , , , , , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2013
|
| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5717756/ https://ncbi.nlm.nih.gov/pubmed/23766104 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/humu.22366 |
| Tagit: |
Lisää tagi
Ei tageja, Lisää ensimmäinen tagi!
|