Fig. 2

Electrophoregrams of the novel heterozygous missense mutation at the 2078 nucleotide position of the MEFV gene. a (red arrow) Normal sequence of unaffected mother and heterozygous mutation c.2078 T > A (p.Met693Lys) of unaffected father. b (red arrow) Heterozygous mutation c.2078 T > A (p.Met693Lys) of our patient, a Moroccan girl presenting with coexistence of familial Mediterranean fever and Behçet’s disease