Mitochondrial diseases are among the most prevalent hereditary metabolic disorders, known to occur in 1 out of every 5,000 births. Single nucleotide variations, indels, and structural variations are ...
Mitochondrial diseases are among the most prevalent hereditary metabolic disorders, known to occur in one out every 5000 births. Single nucleotide variations, indels, and structural variations are ...
Tandem repeats are hard to assess but important regions on the human genome. There are around 200 pathogenic and phenotypic tandem repeats, which are often ignored by standard analysis. Furthermore, ...
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