GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5
GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5
About this item
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Publisher
London: Nature Publishing Group UK
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Language
English
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Publisher
London: Nature Publishing Group UK
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Scope and Contents
Contents
Congenital heart defects (CHDs) are the most common developmental anomaly and are the leading non-infectious cause of mortality in newborns
1
. Only one causative gene,
NKX2-5
, has been identified through genetic linkage analysis of pedigrees with non-syndromic CHDs
2
,
3
. Here, we show that isolated cardiac septal defects...
Alternative Titles
Full title
GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5
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TN_cdi_proquest_miscellaneous_743225092
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_743225092
Other Identifiers
ISSN
0028-0836
E-ISSN
1476-4687
DOI
10.1038/nature01827
