Associated Papers
The role of DUOXA2 in the clinical diagnosis of paediatric congenital hypothyroidism.
Du J et al.
Annals of Medicine, 2025
Complicated Relationship between Genetic Mutations and Phenotypic Characteristics in Transient and Permanent Congenital Hypothyroidism: Analysis of Pooled Literature Data.
Long W et al.
International Journal of Endocrinology, 2020
32565793 (PubMed )
Supplement: 6808517.f1.zip › 6808517.f1 › supplement_table_1.xlsx › Supplement_Table_1
[Characteristics of DUOXA2 gene mutation in children with congenital hypothyroidism].
Tan MY et al.
Zhongguo Dang Dai Er Ke Za Zhi = Chinese Journal of Contemporary Pediatrics, 2017
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