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See Latest ArticlesNovel mitochondrial dna mutations associated with chinese familial hypertrophic cardiomyopathy
Clinical and Experimental Pharmacology and Physiology, 09/10/09
Wei YL et al. – The results of the present study imply that mtDNA mutations G7697A, T12477C and G13135A are genetic factors that indicate a susceptibility to HCM and that could be used for the large–scale screening of genetic markers as well as the early diagnosis of HCM.
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Today in Cardiac/Hypertension...keeping you current
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