Common variation in ISL1 confers genetic susceptibility for human congenital heart disease
Common variation in ISL1 confers genetic susceptibility for human congenital heart disease
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United States: Public Library of Science
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Language
English
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Publisher
United States: Public Library of Science
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Contents
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 ISL1 in cardiac morphogenesis makes this an excepti...
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Full title
Common variation in ISL1 confers genetic susceptibility for human congenital heart disease
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TN_cdi_plos_journals_1292615297
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_1292615297
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ISSN
1932-6203
E-ISSN
1932-6203
DOI
10.1371/journal.pone.0010855
