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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Autors principals: 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.
Format: Artigo
Idioma:Inglês
Publicat: Public Library of Science 2010
Matèries:
Research Article
Accés en línia: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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