Genotypes and phenotypes of congenital goitre and hypothyroidism caused by mutations in dual oxidase 2 genes-Reference-Cited by-同舟云学术

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Genotypes and phenotypes of congenital goitre and hypothyroidism caused by mutations in dual oxidase 2 genes

Published:2014-05-19 Issue:3 Volume:81 Page:452-457
ISSN:0300-0664
Container-title:Clinical Endocrinology
language:en
Short-container-title:Clin Endocrinol

Author:

Wang Fang¹,Lu Kunna¹^ORCID,Yang Zhifeng²,Zhang Shasha³,Lu Wei⁴,Zhang Liqin⁵,Liu Shiguo⁶⁷,Yan Shengli¹

Affiliation:

1. Department of Endocrinology; The Affiliated Hospital of Medical College; Qingdao University; Qingdao China

2. Center of Neonatal screening; Liaocheng Maternal and Child Health; Liaocheng China

3. Department of Endocrinology; Weihai Wendeng Center Hospital; Weihai China

4. Center of Neonatal Screening; Zaozhuang Maternal and Child Health; Zaozhuang China

5. Center of Neonatal screening; Qingdao Maternal and Child Health; Qingdao China

6. Shandong Provincial Key Laboratory of Metabolic Disease; Qingdao China

7. Genetic Laboratory; The Affiliated Hospital of Medical College; Qingdao University; Qingdao China

Funder

National Natural Science Foundation of China

Science and Technology Project by Shandong Provincial Population and Family Planning Commission

Publisher

Wiley

Subject

Endocrinology, Diabetes and Metabolism,Endocrinology

Reference22 articles.

1. Thyroid development and its disorders: genetics and molecular mechanisms;Felice;Endocrine Reviews,2004

2. A 7-year experience with low blood TSH cutoff levels for neonatal screening reveals an unsuspected frequency of congenital hypothyroidism (CH);Corbetta;Clinical Endocrinology (Oxford),2009

3. Genetics and phenomics of hypothyroidism and goiter due to thyroglobulin mutations;Targovnik;Molecular and Cellular Endocrinology,2010

4. Genetics and phenomics of hypothyroidism and goiter due to TPO mutations;Ris-Stalpers;Molecular and Cellular Endocrinology,2010

5. Inactivating mutations in the gene for thyroid oxidase 2 (THOX2) and congenital hypothyroidism;Moreno;The New England Journal of Medicine,2002

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1. Patients with Thyroid Dyshormonogenesis and DUOX2 Variants: Molecular and Clinical Description and Genotype–Phenotype Correlation;International Journal of Molecular Sciences;2024-08-03

2. Clinical and molecular study of patients with thyroid dyshormogenesis and variants in the thyroglobulin gene;Frontiers in Endocrinology;2024-07-08

3. The Severity of Congenital Hypothyroidism With Gland-In-Situ Predicts Molecular Yield by Targeted Next-Generation Sequencing;The Journal of Clinical Endocrinology & Metabolism;2023-03-08

4. Genetic Factors Causing Thyroid Dyshormonogenesis as the Major Etiologies for Primary Congenital Hypothyroidism: Clinical and Genetic Characterization of 33 Patients;Journal of Clinical Medicine;2022-12-09

5. Mutational screening of the TPO and DUOX2 genes in Argentinian children with congenital hypothyroidism due to thyroid dyshormonogenesis;Endocrine;2022-05-04

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