Rare Copy Number Variations in Adults with Tetralogy of Fallot Implicate Novel Risk Gene Pathways
Structural genetic changes, especially copy number variants (CNVs), represent a major source of genetic variation contributing to human disease. Tetralogy of Fallot (TOF) is the most common form of cyanotic congenital heart disease, but to date little is known about the role of CNVs in the etiology...
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| Autors principals: | , , , , , , , , , , , |
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| Format: | Artigo |
| Idioma: | anglès |
| Publicat: |
2012
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| Accés en línia: | https://doi.org/10.1371/journal.pgen.1002843 https://journals.plos.org/plosgenetics/article/file?id=10.1371/journal.pgen.1002843&type=printable |
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