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Mitochondrial DNA somatic mutations (point mutations and large deletions) and mitochondrial DNA variants in human thyroid pathology: a study with emphasis on Hrthle cell tumors

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The other is appearance-related interest, especially skin clarity and overall radiance

In model experiments employing HEK293 cells in a thiamine-deficient medium, the SLC19A1 variant rs1051266:G exhibits a strong decrease in ThDP efflux compared to the canonic SLC19A1 sequence rs1051266:A

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