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GATA5 loss-of-Function Mutations Underlie Tetralogy of Fallot
Tetraology of Fallot (TOF) is the most common form of cyanotic congenital heart disease and is a major cause of significant morbidity and mortality. Emerging evidence demonstrates that genetic risk factors are involved in the pathogenesis of TOF. However, TOF is genetically heterogeneous and the gen...
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Päätekijät: | , , , , , , , |
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Aineistotyyppi: | Artigo |
Kieli: | Inglês |
Julkaistu: |
Ivyspring International Publisher
2012
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Aiheet: | |
Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3534875/ https://ncbi.nlm.nih.gov/pubmed/23289003 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7150/ijms.5270 |
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