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A Novel Homozygous Mutation of Thyroid Peroxidase Gene Abolishes a Disulfide Bond Leading to Congenital Hypothyroidism.
Yakou, Fumiyoshi; Suwanai, Hirotsugu; Ishikawa, Takuya; Itou, Mariko; Shikuma, Jumpei; Miwa, Takashi; Sakai, Hiroyuki; Kanekura, Kohsuke; Narumi, Satoshi; Suzuki, Ryo; Odawara, Masato.
Afiliación
  • Yakou F; Tokyo Medical University, Department of Diabetes, Metabolism and Endocrinology, Tokyo 160-0023, Japan.
  • Suwanai H; Tokyo Medical University, Department of Diabetes, Metabolism and Endocrinology, Tokyo 160-0023, Japan.
  • Ishikawa T; Tokyo Medical University, Department of Diabetes, Metabolism and Endocrinology, Tokyo 160-0023, Japan.
  • Itou M; Tokyo Medical University, Department of Diabetes, Metabolism and Endocrinology, Tokyo 160-0023, Japan.
  • Shikuma J; Tokyo Medical University, Department of Diabetes, Metabolism and Endocrinology, Tokyo 160-0023, Japan.
  • Miwa T; Tokyo Medical University, Department of Diabetes, Metabolism and Endocrinology, Tokyo 160-0023, Japan.
  • Sakai H; Tokyo Medical University, Department of Diabetes, Metabolism and Endocrinology, Tokyo 160-0023, Japan.
  • Kanekura K; Tokyo Medical University, Department of Molecular Pathology, Tokyo 160-8402, Japan.
  • Narumi S; Department of Molecular Endocrinology, National Research Institute for Child Health and Development, Tokyo 157-8535, Japan.
  • Suzuki R; Tokyo Medical University, Department of Diabetes, Metabolism and Endocrinology, Tokyo 160-0023, Japan.
  • Odawara M; Tokyo Medical University, Department of Diabetes, Metabolism and Endocrinology, Tokyo 160-0023, Japan.
Int J Endocrinol ; 2020: 9132372, 2020.
Article en En | MEDLINE | ID: mdl-32908504

Texto completo: 1 Base de datos: MEDLINE Tipo de estudio: Screening_studies Idioma: En Revista: Int J Endocrinol Año: 2020 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Tipo de estudio: Screening_studies Idioma: En Revista: Int J Endocrinol Año: 2020 Tipo del documento: Article