Common Variation in ISL1 Confers Genetic Susceptibility for Human Congenital Heart Disease

Congenital heart disease (CHD) is the most common birth abnormality and the etiology is unknown in the overwhelming majority of cases. ISLET1 (ISL1) is a transcription factor that marks cardiac progenitor cells and generates diverse multipotent cardiovascular cell lineages. The fundamental role of I...

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Bibliografiset tiedot
Päätekijät: Stevens, Kristen N., Hakonarson, Hakon, Kim, Cecilia E., Doevendans, Pieter A., Koeleman, Bobby P. C., Mital, Seema, Raue, Jennifer, Glessner, Joseph T., Coles, John G., Moreno, Victor, Granger, Anne, Gruber, Stephen B., Gruber, Peter J.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Public Library of Science 2010
Aiheet:
Research Article
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC2877111/
https://ncbi.nlm.nih.gov/pubmed/20520780
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0010855
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