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Fig. 2 | BMC Medical Genetics

Fig. 2

From: Associations of mitochondrial DNA 3777–4679 region mutations with maternally inherited essential hypertensive subjects in China

Fig. 2

a. Identification of the m.3970C > T mutation in the mitochondrial ND1 gene. Arrow indicates the position of the gene mutation. b. Identification of the m.4248 T > C mutation in the mitochondrial ND1 gene. Arrow indicates the position of the gene mutation. c. Identification of the m.4563 delG mutation. Arrow indicates the position of the deletion mutation. d. Identification of the m.4611delA mutations. Arrow indicates the position of the deletion mutation

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BMC Medical Genetics

ISSN: 1471-2350

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