Genotype and phenotype correlation in a cohort of Chinese congenital hypothyroidism patients with DUOX2 mutations.

Zheng, Zhangqian; Yang, Lin; Sun, Chengjun; Wu, Jing; Luo, Feihong; Zhou, Wenhao; Lu, Wei

Zheng, Zhangqian; Yang, Lin; Sun, Chengjun; Wu, Jing; Luo, Feihong; Zhou, Wenhao; Lu, Wei.

Afiliação

Zheng Z; Department Endocrinology and Inherited Metabolic Diseases, Children's Hospital of Fudan University, Shanghai, China.
Yang L; Department Endocrinology and Inherited Metabolic Diseases, Children's Hospital of Fudan University, Shanghai, China.
Sun C; Department Endocrinology and Inherited Metabolic Diseases, Children's Hospital of Fudan University, Shanghai, China.
Wu J; Department Endocrinology and Inherited Metabolic Diseases, Children's Hospital of Fudan University, Shanghai, China.
Luo F; Department Endocrinology and Inherited Metabolic Diseases, Children's Hospital of Fudan University, Shanghai, China.
Zhou W; Department Endocrinology and Inherited Metabolic Diseases, Children's Hospital of Fudan University, Shanghai, China.
Lu W; Department Endocrinology and Inherited Metabolic Diseases, Children's Hospital of Fudan University, Shanghai, China.

Ann Transl Med ; 8(24): 1649, 2020 Dec.

Article em En | MEDLINE | ID: mdl-33490161

Palavras-chave

Chinese; Congenital hypothyroidism (CH); dual oxidase 2 (DUOX2); phenotype genotype

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Ann Transl Med Ano de publicação: 2020 Tipo de documento: Article País de afiliação: China

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