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Autor:
Qi-Zhu Wu, Diane Fatkin, Nicolas Plachta, Anjana Chandran, Stephanie E. Simonds, Milena B. Furtado, Nadia Rosenthal, James T. Pearson, Christine Biben, David Willians, Taylor J. Willow, Gurpreet Kaur, Joelle Perera, Hieu T. Nim, Richard P. Harvey, Julia C. Wilmanns, Ekaterina Salimova, James M. Denegre, Olivia Hon, David M. Kaye, Mirana Ramialison, Stephen A. Murray, Mauro W. Costa, Michael A. Cowley
Mutations in the Nkx2-5 gene are a main cause of congenital heart disease. Several studies have addressed the phenotypic consequences of disrupting the Nkx2-5 gene locus, although animal models to date failed to recapitulate the full spectrum of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f696b31663b1143e8fa0f2aa2167515e
http://hdl.handle.net/10044/1/56521
http://hdl.handle.net/10044/1/56521