Molecular and Clinical Features of Congenital Hypothyroidism Due to Multiple <i>DUOX2</i> Variants-Reference-Cited by-同舟云学术

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Molecular and Clinical Features of Congenital Hypothyroidism Due to Multiple DUOX2 Variants

Published:2024-07-01 Issue:7 Volume:34 Page:827-836
ISSN:1050-7256
Container-title:Thyroid®
language:en
Short-container-title:Thyroid®

Author:

Uehara Erika¹²,Abe Kiyomi³⁴,Tanase-Nakao Kanako¹,Muroya Koji⁵,Hattori Atsushi¹⁶,Matsubara Keiko¹⁶,Fukami Maki¹⁶,Narumi Satoshi¹³

Affiliation:

1. Department of Molecular Endocrinology, National Research Institute for Child Health and Development, Tokyo, Japan.

2. Department of Advanced Pediatric Medicine, Tohoku University School of Medicine, Tokyo, Japan.

3. Department of Pediatrics, Keio University School of Medicine, Tokyo, Japan.

4. Department of Pediatrics, Tokyo Saiseikai Central Hospital, Tokyo, Japan.

5. Department of Endocrinology and Metabolism, Kanagawa Children’s Medical Center, Yokohama, Japan.

6. Division of Diversity Research, National Research Institute for Child Health and Development, Tokyo, Japan.

Publisher

Mary Ann Liebert Inc

Link

https://www.liebertpub.com/doi/pdf/10.1089/thy.2024.0046

Reference27 articles.

1. Defects of thyroidal hydrogen peroxide generation in congenital hypothyroidism

2. Identification of the Maturation Factor for Dual Oxidase

3. Molecular Basis of Thyroid Dyshormonogenesis: Genetic Screening in Population-Based Japanese Patients

4. MECHANISMS IN ENDOCRINOLOGY: The pathophysiology of transient congenital hypothyroidism

5. Inactivating Mutations in the Gene for Thyroid Oxidase 2 (THOX2) and Congenital Hypothyroidism

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