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Next-generation sequencing of NKX2.1 , FOXE1 , PAX8 , NKX2.5 , and TSHR in 100 Chinese patients with congenital hypothyroidism and athyreosis

Next-generation SequencingGeneticsThyroid DiseaseImmunologyPathologyNeurogeneticsThyroid DisordersCongenital HypothyroidismThyroid HormoneMedicineMolecular MedicineChinese Patients