Fig. 5From: Multicentric carpotarsal osteolysis syndrome with variants of MAFB gene: a case report and literature reviewPedigree and MAFB partial electropherograms. Family pedigree (A), DNA sequencing from his father (B), his mother (C), his healthy sibling (D), and the proband (E) demonstrating a heterozygous missense mutation at nucleotide 206 from C to T (c.206 C > T) that predicts the change of amino acid at codon 69 from serine to leucine (p.Ser69Leu)Back to article page