Single allele mutations at the heart of congenital disease
Open Access
- 1 December 1999
- journal article
- editorial
- Published by American Society for Clinical Investigation in Journal of Clinical Investigation
- Vol. 104 (11) , 1483-1484
- https://doi.org/10.1172/jci8825
Abstract
No abstract availableThis publication has 9 references indexed in Scilit:
- To be or not to be active: the stochastic nature of enhancer actionBioEssays, 2000
- Mutations in the cardiac transcription factor NKX2.5 affect diverse cardiac developmental pathwaysJournal of Clinical Investigation, 1999
- Independent regulation of the two Pax5 alleles during B-cell developmentNature Genetics, 1999
- Different TBX5 interactions in heart and limb defined by Holt–Oram syndrome mutationsProceedings of the National Academy of Sciences, 1999
- Tinman Function Is Essential for Vertebrate Heart Development: Elimination of Cardiac Differentiation by Dominant Inhibitory Mutants of thetinman-Related Genes,XNkx2-3andXNkx2-5Developmental Biology, 1998
- Vertebrate tinman homologues XNkx2-3 and XNkx2-5 are required for heart formation in a functionally redundant mannerDevelopment, 1998
- Congenital Heart Disease Caused by Mutations in the Transcription Factor NKX2-5Science, 1998
- Reduced Penetrance, Variable Expressivity, and Genetic Heterogeneity of Familial Atrial Septal DefectsCirculation, 1998
- NK-2Homeobox Genes and Heart DevelopmentDevelopmental Biology, 1996