Identification of Novel Causal FBN1 Mutations in Pedigrees of Marfan Syndrome

<div>Predicted results for the frameshift variants by Swiss-Model. (a) Predicted 3D model of the variant (c.4282 delC.) in family 1. (b) Predicted 3D model of the variant (c.2192 delC.) in family 3.</div>

International Journal of Genomics

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Figure 4

Figure 4: Identification of Novel Causal FBN1 Mutations in Pedigrees of Marfan Syndrome 