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Mutations in SDHD, a mitochondrial complex II gene, in hereditary paraganglioma

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Our data suggested that mutation of 3UTR-1 had no obvious effect to rescue the phenotype caused by DDX3X or METTL16 deficiency, whereas mutation of 3UTR-2 or 3UTR-3 fully eliminated the outcome induced by DDX3X or METTL16 inhibition (Fig