Fig. 2From: Analysis of association among clinical features and shorter leukocyte telomere length in mitochondrial diabetes with m.3243A>G mitochondrial DNA mutationa Pedigree of family I. b Pedigree of family II. c Pedigree of family III. d Pedigree of family IV. e Pedigree of family V. Show the patient with maternally inherited diabetes and deafness, Show family member without the disease. Shows the proband in the family. II1 in family II and II1 in family IV have MELAS and mitochondrial diabetes. III1 in family II has mt DNA 3243 mutation, although he did not have symptoms of mitochondrial diabetesBack to article page