Reamon-Buettner, S. M., Sattlegger, E., Ciribilli, Y., Inga, A., Wessel, A., & Borlak, J. (2013). Transcriptional Defect of an Inherited NKX2-5 Haplotype Comprising a SNP, a Nonsynonymous and a Synonymous Mutation, Associated with Human Congenital Heart Disease. Public Library of Science.

Reamon-Buettner, Stella Marie, Evelyn Sattlegger, Yari Ciribilli, Alberto Inga, Armin Wessel, và Jürgen Borlak. Transcriptional Defect of an Inherited NKX2-5 Haplotype Comprising a SNP, a Nonsynonymous and a Synonymous Mutation, Associated With Human Congenital Heart Disease. Public Library of Science, 2013.

Reamon-Buettner, Stella Marie, et al. Transcriptional Defect of an Inherited NKX2-5 Haplotype Comprising a SNP, a Nonsynonymous and a Synonymous Mutation, Associated With Human Congenital Heart Disease. Public Library of Science, 2013.