Your browser doesn't support javascript.
loading
Functional analysis of thyroid peroxidase gene mutations resulting in congenital hypothyroidism.
Zhao, Defa; Li, Yang; Shan, Zhongyan; Teng, Weiping; Li, Jing; Teng, Xiaochun.
Afiliación
  • Zhao D; Department of Endocrinology and Metabolism, Institute of Endocrine, Liaoning Provincial Key Laboratory of Endocrine Diseases, The First Hospital of China Medical University, Shenyang, China.
  • Li Y; Department of Endocrinology and Metabolism, Institute of Endocrine, Liaoning Provincial Key Laboratory of Endocrine Diseases, The First Hospital of China Medical University, Shenyang, China.
  • Shan Z; Department of Endocrinology and Metabolism, Institute of Endocrine, Liaoning Provincial Key Laboratory of Endocrine Diseases, The First Hospital of China Medical University, Shenyang, China.
  • Teng W; Department of Endocrinology and Metabolism, Institute of Endocrine, Liaoning Provincial Key Laboratory of Endocrine Diseases, The First Hospital of China Medical University, Shenyang, China.
  • Li J; Department of Endocrinology and Metabolism, Institute of Endocrine, Liaoning Provincial Key Laboratory of Endocrine Diseases, The First Hospital of China Medical University, Shenyang, China.
  • Teng X; Department of Endocrinology and Metabolism, Institute of Endocrine, Liaoning Provincial Key Laboratory of Endocrine Diseases, The First Hospital of China Medical University, Shenyang, China.
Clin Endocrinol (Oxf) ; 93(4): 499-507, 2020 10.
Article en En | MEDLINE | ID: mdl-32424871
Asunto(s)
Palabras clave
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Hipotiroidismo Congénito Límite: Adult / Female / Humans / Infant Idioma: En Revista: Clin Endocrinol (Oxf) Año: 2020 Tipo del documento: Article País de afiliación: China
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Hipotiroidismo Congénito Límite: Adult / Female / Humans / Infant Idioma: En Revista: Clin Endocrinol (Oxf) Año: 2020 Tipo del documento: Article País de afiliación: China