Missense Mutations in the PTPN11 as a Cause of Cardiac Defects Associated with Noonan Syndrome

Pogue Distinguished Chair in Research on Cardiac Birth Defects, Joel B. Steinberg, M.D. Chair in Pediatrics Professor, Departments of Pediatrics and Molecular Biology, University of Texas, Southwestern Medical Center at Dallas

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Makoto Nakazawa MD,

Makoto Nakazawa MD

Professor and Head, Pediatric Cardiology, The Heart Institute of Japan, Tokyo Women's Medical University

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First published: 01 January 2005

https://doi.org/10.1002/9780470988664.ch66

Citations: 1

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References

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Cardiovascular Development and Congenital Malformations: Molecular & Genetic Mechanisms

Missense Mutations in the PTPN11 as a Cause of Cardiac Defects Associated with Noonan Syndrome

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Missense Mutations in the PTPN11 as a Cause of Cardiac Defects Associated with Noonan Syndrome

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