Related Experiment Video

Updated: May 19, 2026

In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila
06:41

In Vivo Functional Study of Disease-associated Rare Human Variants Using Drosophila

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Novel Variants in the SLC16A2 Gene Associated With Allan-Herndon-Dudley Syndrome in China

Wei Li1, Zijia Sun1, Xiao Wu1

  • 1Department of Rehabilitation, Children's Hospital of Nanjing Medical University, College of Pediatrics, Nanjing Medical University, Nanjing, Jiangsu, China, njmu.edu.cn.

Human Mutation
|May 18, 2026
PubMed
Abstract

Keywords:
Allan–Herndon–Dudley syndromeSLC16A2 genemonocarboxylate Transporter 8thyroid hormone

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