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Two novel TSHR gene mutations (p.R528C and c.392+4del4) associated with congenital hypothyroidism.
Qiu, Ya-Li; Ma, Shao-Gang; Liu, Hong; Yue, Hong-Ni.
Affiliation
  • Qiu YL; a Department of Neonatal Screening and Care , Women and Children's Hospital of Suqian , Suqian , China.
  • Ma SG; b Department of Endocrinology and Metabolism , Huai'an Hospital Affiliated to Xuzhou Medical College and Huai'an Second People's Hospital , Huai'an , China.
  • Liu H; b Department of Endocrinology and Metabolism , Huai'an Hospital Affiliated to Xuzhou Medical College and Huai'an Second People's Hospital , Huai'an , China.
  • Yue HN; c Department of Children Healthcare , Women and Children's Hospital of Huai'an , Huai'an Jiangsu , China.
Endocr Res ; 41(3): 180-4, 2016 Aug.
Article in En | MEDLINE | ID: mdl-26864598
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Receptors, Thyrotropin / Congenital Hypothyroidism Type of study: Risk_factors_studies Limits: Child / Child, preschool / Female / Humans / Male Language: En Journal: Endocr Res Journal subject: ENDOCRINOLOGIA Year: 2016 Document type: Article Affiliation country: China Country of publication: United kingdom
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Receptors, Thyrotropin / Congenital Hypothyroidism Type of study: Risk_factors_studies Limits: Child / Child, preschool / Female / Humans / Male Language: En Journal: Endocr Res Journal subject: ENDOCRINOLOGIA Year: 2016 Document type: Article Affiliation country: China Country of publication: United kingdom