Case Reports in Genetics / 2013 / Article / Fig 3

Case Report

A Novel De Novo EFNB1 Gene Mutation in a Mexican Patient with Craniofrontonasal Syndrome

Figure 3

In silico analysis using PolyPhen-2 software shows that change in p.M158T is pathogenic (a) and predicted to be highly conserved in different species (b).
349725.fig.003a
(a)
349725.fig.003b
(b)

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