Figure 2 | European Journal of Human Genetics

Figure 2

From: The tRNAMet 4435A>G mutation in the mitochondrial haplogroup G2a1 is responsible for maternally inherited hypertension in a Chinese pedigree

Figure 2

Identification of the 4435A>G mutation in the mitochondrial tRNAMet gene. (a) Partial sequence chromatograms of the tRNAMet gene from affected individual II-6 and a married-in control II-7. An arrow indicates the location of the base changes at position 4435. (b) The location of the 4435A>G mutation in the mitochondrial tRNAMet. The cloverleaf structure of human mitochondrial tRNAMet is derived from Florentz et al32 Arrowhead indicates the position of the 4435A>G mutation.

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