Article

Mutation Screening of DUOX2 Gene in Children with Congenital Hypothyroidism

2020-01-30

Abstract excerpt

<title>Abstract</title> <p>Background: Congenital hypothyroidism(CH) is generally known as the most common neonatal endocrine disorder. However, the mutational spectrum of DUOX2 gene and the relationship between genotype and phenotype have not been fully established among Chinese CH patients. Therefore, The aim of this study was to screen DUOX2 mutations in Chinese patients with CH and to research the relationshi...

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Literature Corpus work: b0c54ba5-4e20-5f40-9761-1f6fe4ba9da1
DOI: 10.21203/rs.2.22276/v1

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