Functional Characterization of a Novel Mutation in NKX2-5 Associated with Congenital Heart Disease and Adult-Onset Cardiomyopathy

av Costa, Mauro W., Guo, Guanglan, Wolstein, Orit, Vale, Molly, Castro, M. Leticia, Wang, Libin, Otway, Robyn, Riek, Peter, Cochrane, Natalie, Furtado, Milena, Semsarian, Christopher, Weintraub, Robert G., Yeoh, Thomas, Hayward, Christopher, Keogh, Anne, Macdonald, Peter, Feneley, Michael, Graham, Robert M., Seidman, Jonathan G., Seidman, Christine E., Rosenthal, Nadia, Fatkin, Diane, Harvey, Richard P.
Publicerad 2013