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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Detalles Bibliográficos
Autores principales: 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.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2877111/
https://www.ncbi.nlm.nih.gov/pubmed/20520780
http://dx.doi.org/10.1371/journal.pone.0010855

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2877111/
https://www.ncbi.nlm.nih.gov/pubmed/20520780
http://dx.doi.org/10.1371/journal.pone.0010855

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