Mitochondrial T16189C Polymorphism Is Associated with Metabolic Syndrome in the Mexican Population

<div>Detection of mitochondrial DNA (mtDNA) T16189 C polymorphism (a) 3% agarose gel  (1) molecular marker,  (2) no template PCR control, and (3–9) amplicons obtained from representative samples. (b, c) Wild-type sequence and mtDNA T16189C polymorphism, respectively. The arrows indicated the variants detected.</div>

Disease Markers

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Figure 1

Figure 1: Mitochondrial T16189C Polymorphism Is Associated with Metabolic Syndrome in the Mexican Population 