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Transcriptional Defect of an Inherited NKX2-5 Haplotype Comprising a SNP,a Nonsynonymous and a Synonymous Mutation,Associated with Human Congenital Heart Disease |
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| Authors: | Stella Marie Reamon-Buettner Evelyn Sattlegger Yari Ciribilli Alberto Inga Armin Wessel Jürgen Borlak |
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