Somatic NKX2-5 mutations as a novel mechanism of disease in complex congenital heart disease | Journal of Medical Genetics

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Somatic NKX2-5 mutations as a novel mechanism of disease in complex congenital heart disease

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Cite this article as:: Reamon-Buettner SM, Borlak J

Somatic NKX2-5 mutations as a novel mechanism of disease in complex congenital heart disease

Journal of Medical Genetics 2004;41:684-690.