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DUOX2 variants are a frequent cause of congenital primary hypothyroidism in Thai patients

29 Oct 2020

Abstract excerpt

OBJECTIVE: To identify the genetic etiologies of congenital primary hypothyroidism (CH) in Thai patients. DESIGN AND METHODS: CH patients were enrolled. Clinical characteristics including age, signs and symptoms of CH, pedigree, family history, screened thyroid-stimulating hormone results, thyroid function tests, thyroid imaging, clinical course and treatment of CH were collected. Clinical exome sequencing by...

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PMID: 33310921
DOI: 10.1530/ec-20-0411

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