Point mutations in murine Nkx2-5 phenocopy human congenital heart disease and induce pathogenic Wnt signaling.
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Milena B. Furtado | Mauro W. Costa | S. Murray | N. Rosenthal | D. Fatkin | Qizhu Wu | C. Biben | M. Ramialison | R. Harvey | D. Kaye | N. Plachta | G. Kaur | E. Salimova | J. Denegre | J. Pearson | Anjana Chandran | Stephanie E. Simonds | H. Nim | Michael Cowley | Olivia Hon | J. Wilmanns | Joelle Perera | Taylor J Willow | David Willians | Qizhu Wu | David R. A. Willians