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Specific genetic aberrations of parathyroid in Chinese patients with tertiary hyperparathyroidism using whole-exome sequencing.

Front Endocrinol (Lausanne) · 2023 · PMC10579901 · PMID 37854190

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Notably, the expression levels of PRKDC, TBX20, and NOX3 in hyperplastic parathyroids of THPT with exon mutations were relatively lower compared to those without mutations, although the difference did not reach statistical significance ( Figure 3B ).

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