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. Author manuscript; available in PMC: 2012 May 1.
Published in final edited form as: Cardiovasc Pathol. 2011 Jan 22;20(3):168–176. doi: 10.1016/j.carpath.2010.11.007

Figure 3.

Figure 3

The autosomal–dominant inheritance of the disease phenotype with complete penetrance of the Notch1 loss of function mutation22. The Notch1 mutations segregate with the family members with aortic valve disease. There are also family members who expressed congenital heart abnormalities. (Used with Permission from Nature Publishing Group, Publisher for Nature.)