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A novel c.1391_1428delinsT mutation in TSHR as a cause of familial congenital hypothyroidism with delayed onset.
Watanabe, Daisuke; Yagasaki, Hideaki; Ishii, Sayaka; Mitsui, Yumiko; Nakane, Takaya; Inukai, Takeshi.
Affiliation
  • Watanabe D; Department of Pediatrics, Faculty of Medicine, University of Yamanashi, Yamanashi, Japan. Electronic address: dwatanabe@yamanashi.ac.jp.
  • Yagasaki H; Department of Pediatrics, Faculty of Medicine, University of Yamanashi, Yamanashi, Japan.
  • Ishii S; Department of Pediatrics, Faculty of Medicine, University of Yamanashi, Yamanashi, Japan.
  • Mitsui Y; Department of Pediatrics, Faculty of Medicine, University of Yamanashi, Yamanashi, Japan.
  • Nakane T; Department of Pediatrics, Faculty of Medicine, University of Yamanashi, Yamanashi, Japan.
  • Inukai T; Department of Pediatrics, Faculty of Medicine, University of Yamanashi, Yamanashi, Japan.
Pediatr Neonatol ; 61(1): 114-116, 2020 02.
Article in En | MEDLINE | ID: mdl-31836301
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Pediatr Neonatol Year: 2020 Document type: Article Country of publication: Singapore
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Pediatr Neonatol Year: 2020 Document type: Article Country of publication: Singapore