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Diagnosis, treatment and genetic analysis of 11ß -hydroxylase deficiency caused by CYP11B gene mutation.
Song, Qing-Qing; Zhang, Su-Su; Zhang, Zhen; Sun, Jia; Yang, Rui; Li, Ji-Tong; Chen, Hong.
Afiliação
  • Song QQ; 1. Department of Endocrinology and Metabolism, Zhujiang Hospital of Southern Medical University, Guangzhou 510282, China.
  • Zhang SS; 2. Department of Endocrinology and Metabolism, Zhanjiang Central People's Hospital, Zhanjiang 524037, China.
  • Zhang Z; 1. Department of Endocrinology and Metabolism, Zhujiang Hospital of Southern Medical University, Guangzhou 510282, China.
  • Sun J; 1. Department of Endocrinology and Metabolism, Zhujiang Hospital of Southern Medical University, Guangzhou 510282, China.
  • Yang R; 1. Department of Endocrinology and Metabolism, Zhujiang Hospital of Southern Medical University, Guangzhou 510282, China.
  • Li JT; 1. Department of Endocrinology and Metabolism, Zhujiang Hospital of Southern Medical University, Guangzhou 510282, China.
  • Chen H; 1. Department of Endocrinology and Metabolism, Zhujiang Hospital of Southern Medical University, Guangzhou 510282, China.
Yi Chuan ; 44(12): 1175-1182, 2022 Dec 20.
Article em En | MEDLINE | ID: mdl-36927563
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Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Esteroide 11-beta-Hidroxilase / Hiperplasia Suprarrenal Congênita Tipo de estudo: Diagnostic_studies Limite: Adolescent / Humans Idioma: En Revista: Yi Chuan Assunto da revista: GENETICA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: China
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Esteroide 11-beta-Hidroxilase / Hiperplasia Suprarrenal Congênita Tipo de estudo: Diagnostic_studies Limite: Adolescent / Humans Idioma: En Revista: Yi Chuan Assunto da revista: GENETICA Ano de publicação: 2022 Tipo de documento: Article País de afiliação: China