Common and Rare <i>DUOX</i> Variants in Patients With Congenital Hypothyroidism: Case-control Study and Family-based Analysis
Our research confirmed that DUOX variants are inherited in an autosomal recessive manner. We present a comprehensive spectrum of rare and common DUOX variants that provides more accurate insights into the pathogenesis of CH associated with DUOX.
Authors
- Fengqi Wang (ORCID: https://orcid.org/0000-0002-4609-0983)
- Yanan Duan (ORCID: https://orcid.org/0000-0002-2766-8583)
- Shiguo Liu (ORCID: https://orcid.org/0000-0003-4026-4046)
- Hui Zou (ORCID: https://orcid.org/0000-0001-9782-0475)
- Xiangju Liu (ORCID: https://orcid.org/0000-0003-4462-7879)
- Xiaoyu Wang (ORCID: https://orcid.org/0000-0002-4696-5460)
- Yaning Jia
- Miaomiao Li (ORCID: https://orcid.org/0000-0003-1290-7120)
- Liqin Zhang (ORCID: https://orcid.org/0000-0003-4812-6617)
Institutions
- Qingdao University (CN)
- Jinan Maternity And Care Hospital (CN)
- People’s Hospital of Rizhao (CN)
- Taiyuan Maternity and Child Care Hospital (CN)
- Affiliated Hospital of Qingdao University (CN)
- Qingdao Women and Children's Hospital (CN)
Publication Details
- Journal
- The Journal of Clinical Endocrinology & Metabolism
- Published
- 2025-02-19
- DOI
- https://doi.org/10.1210/clinem/dgaf109
- Citations
- 2
- Primary Topic
- Thyroid Disorders and Treatments
- Type
- article
- Field-Weighted Citation Impact
- 2.59