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. 2017 Feb 23;18:20. doi: 10.1186/s12881-017-0380-0

Fig. 1.

Fig. 1

a Schematic representation of the family tree with the distribution of HHT and normal relatives. b Clinical diagnostic criteria of the affected relatives. c Mutated sequence corresponding to this particular HHT family, showing the nucleotide substitution c.-58 G > A at the proximal promoter of Endoglin. Arrows point to the two unaffected individuals, who were also sequenced