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Reamon-Buettner, S.M., Sattlegger, E., Ciribilli, Y., Inga, A., Wessel, A. and 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. PLoS ONE, 8, e83295.
https://doi.org/10.1371/journal.pone.0083295

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