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See Latest ArticlesFailures in Mitochondrial tRNAMet and tRNAGln Metabolism Caused by the Novel 4401A>G Mutation Are Involved in Essential Hypertension in a Han Chinese Family
Hypertension, 06/23/09
Li R et al. - The data suggest that mitochondrial dysfunctions, caused by the 4401A>G mutation, are involved in the development of hypertension in this Chinese pedigree.
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Association of the PPARGC1A Gene Polymorphism With Diabetic Nephropathy in an Asian Indian Population (CURES-41)
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Today in Hypertension...keeping you current
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Managing Peripheral Edema in Patients With Arterial Hypertension
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