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A case of MODY5-like manifestations without mutations or deletions in coding and minimal promoter regions of the HNF1B gene.
Kuwabara-Ohmura, Yayoi; Iizuka, Katsumi; Liu, Yanyan; Takao, Ken; Nonomura, Kenta; Kato, Takehiro; Mizuno, Masami; Hosomichi, Kazuyoshi; Tajima, Atsushi; Miyazaki, Tatsuhiko; Horikawa, Yukio; Yabe, Daisuke.
Afiliação
  • Kuwabara-Ohmura Y; Department of Diabetes and Endocrinology, Gifu University Graduate School of Medicine, Gifu 501-1194, Japan.
  • Iizuka K; Department of Diabetes and Endocrinology, Gifu University Graduate School of Medicine, Gifu 501-1194, Japan.
  • Liu Y; Department of Diabetes and Endocrinology, Gifu University Graduate School of Medicine, Gifu 501-1194, Japan.
  • Takao K; Department of Diabetes and Endocrinology, Gifu University Graduate School of Medicine, Gifu 501-1194, Japan.
  • Nonomura K; Department of Diabetes and Endocrinology, Gifu University Graduate School of Medicine, Gifu 501-1194, Japan.
  • Kato T; Department of Diabetes and Endocrinology, Gifu University Graduate School of Medicine, Gifu 501-1194, Japan.
  • Mizuno M; Department of Diabetes and Endocrinology, Gifu University Graduate School of Medicine, Gifu 501-1194, Japan.
  • Hosomichi K; Department of Bioinformatics and Genomics, Graduate School of Advanced Preventive Medical Sciences, Kanazawa University, Kanazawa 920-8640, Japan.
  • Tajima A; Department of Bioinformatics and Genomics, Graduate School of Advanced Preventive Medical Sciences, Kanazawa University, Kanazawa 920-8640, Japan.
  • Miyazaki T; Pathology Division, Gifu University Hospital, Gifu 501-1194, Japan.
  • Horikawa Y; Department of Diabetes and Endocrinology, Gifu University Graduate School of Medicine, Gifu 501-1194, Japan.
  • Yabe D; Department of Diabetes and Endocrinology, Gifu University Graduate School of Medicine, Gifu 501-1194, Japan.
Endocr J ; 67(9): 981-988, 2020 Sep 28.
Article em En | MEDLINE | ID: mdl-32461507

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças do Sistema Nervoso Central / Regiões Promotoras Genéticas / Esmalte Dentário / Diabetes Mellitus Tipo 2 / Doenças Renais Císticas / Fator 1-beta Nuclear de Hepatócito / Mutação Limite: Aged / Female / Humans Idioma: En Revista: Endocr J Assunto da revista: ENDOCRINOLOGIA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Japão

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Doenças do Sistema Nervoso Central / Regiões Promotoras Genéticas / Esmalte Dentário / Diabetes Mellitus Tipo 2 / Doenças Renais Císticas / Fator 1-beta Nuclear de Hepatócito / Mutação Limite: Aged / Female / Humans Idioma: En Revista: Endocr J Assunto da revista: ENDOCRINOLOGIA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Japão