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Endocrinology
Genetic Basis of Congenital Central Hypothyroidism in Children: Expanding the Mutational Spectrum of POU1F1 and ATP6V0A4
Chunyun Fu1 Medical Science Laboratory, Children’s Hospital, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region, Nanning, 530003, People’s Republic of ChinaCorrespondence[email protected]
https://orcid.org/0000-0001-5302-3845View further author information
Jingsi Luo2 Department of Genetic Metabolism, Children’s Hospital, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region, Nanning, 530003, People’s Republic of ChinaView further author information
, Jiasun Su2 Department of Genetic Metabolism, Children’s Hospital, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region, Nanning, 530003, People’s Republic of ChinaView further author information
, Shujie Zhang2 Department of Genetic Metabolism, Children’s Hospital, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region, Nanning, 530003, People’s Republic of ChinaView further author information
, Qi Yang2 Department of Genetic Metabolism, Children’s Hospital, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region, Nanning, 530003, People’s Republic of ChinaView further author information
& Yue Zhang2 Department of Genetic Metabolism, Children’s Hospital, Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region, Nanning, 530003, People’s Republic of ChinaView further author information
Pages 3355-3362
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Received 23 May 2023, Accepted 01 Aug 2023, Published online: 08 Aug 2023
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