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A multigenerational study on phenotypic consequences of the most common causal variant of HNF1A-MODY.
Kettunen, Jarno L T; Rantala, Elina; Dwivedi, Om P; Isomaa, Bo; Sarelin, Leena; Kokko, Paula; Hakaste, Liisa; Miettinen, Päivi J; Groop, Leif C; Tuomi, Tiinamaija.
Afiliação
  • Kettunen JLT; Folkhälsan Research Center, Helsinki, Finland.
  • Rantala E; Institute for Molecular Medicine Finland (FIMM), University of Helsinki, Helsinki, Finland.
  • Dwivedi OP; Department of Endocrinology, Abdominal Center, Helsinki University Hospital, Helsinki, Finland.
  • Isomaa B; Research Programs Unit, Clinical and Molecular Metabolism, University of Helsinki, Helsinki, Finland.
  • Sarelin L; Vantaa Healthcare Center, Vantaa, Finland.
  • Kokko P; Institute for Molecular Medicine Finland (FIMM), University of Helsinki, Helsinki, Finland.
  • Hakaste L; Folkhälsan Research Center, Helsinki, Finland.
  • Miettinen PJ; Folkhälsan Research Center, Helsinki, Finland.
  • Groop LC; Folkhälsan Research Center, Helsinki, Finland.
  • Tuomi T; Institute for Molecular Medicine Finland (FIMM), University of Helsinki, Helsinki, Finland.
Diabetologia ; 65(4): 632-643, 2022 04.
Article em En | MEDLINE | ID: mdl-34951657
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Diabetes Mellitus Tipo 2 / Fator 1-alfa Nuclear de Hepatócito Tipo de estudo: Prognostic_studies Limite: Adult / Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Diabetes Mellitus Tipo 2 / Fator 1-alfa Nuclear de Hepatócito Tipo de estudo: Prognostic_studies Limite: Adult / Humans Idioma: En Ano de publicação: 2022 Tipo de documento: Article