Fig. 1
From: Maternally inherited coronary heart disease is associated with a novel mitochondrial tRNA mutation
The Chinese pedigree with CHD. a Vision-impaired individuals are indicated by blackened symbols. b Identification of the 15910C > T mutation in the tRNA gene. Partial sequences chromatograms of tRNA gene from the proband and one Chinese control. c The location of the 15910C > T mutation in the mitochondrial tRNAThr. An arrow indicates the location of the base changes at position 15,910