Haploinsufficiency of the <i>NF1</i> gene is associated with protection against diabetes.

Kallionpää, Roope A; Peltonen, Sirkku; Leppävirta, Jussi; Pöyhönen, Minna; Auranen, Kari; Järveläinen, Hannu; Peltonen, Juha

Haploinsufficiency of the NF1 gene is associated with protection against diabetes.

Kallionpää, Roope A; Peltonen, Sirkku; Leppävirta, Jussi; Pöyhönen, Minna; Auranen, Kari; Järveläinen, Hannu; Peltonen, Juha.

Afiliación

Kallionpää RA; Institute of Biomedicine, University of Turku, Turku, Finland.
Peltonen S; Department of Dermatology and Venereology, University of Turku, Turku, Finland.
Leppävirta J; Department of Dermatology, Turku University Hospital, Turku, Finland.
Pöyhönen M; Department of Clinical Genetics, HUSLAB, Helsinki University Hospital (HUS) Diagnostic Center, Helsinki, Finland.
Auranen K; Department of Medical and Clinical Genetics, University of Helsinki, Helsinki, Finland.
Järveläinen H; Department of Clinical Genetics, HUSLAB, Helsinki University Hospital (HUS) Diagnostic Center, Helsinki, Finland.
Peltonen J; Department of Medical and Clinical Genetics, University of Helsinki, Helsinki, Finland.

J Med Genet ; 58(6): 378-384, 2021 06.

Article en En | MEDLINE | ID: mdl-32571896

Asunto(s)

Diabetes Mellitus Tipo 2/genética; Genes de Neurofibromatosis 1; Haploinsuficiencia; Neurofibromatosis 1/genética; Adulto; Niño; Estudios de Cohortes; Femenino; Predisposición Genética a la Enfermedad; Humanos; Masculino; Persona de Mediana Edad; Modelos de Riesgos Proporcionales

Palabras clave

autoimmune diseases; congenital, hereditary, and neonatal diseases and abnormalities; diabetes mellitus; genetic association studies; genetic predisposition to disease

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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Genes de Neurofibromatosis 1 / Neurofibromatosis 1 / Diabetes Mellitus Tipo 2 / Haploinsuficiencia Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adult / Child / Female / Humans / Male / Middle aged Idioma: En Revista: J Med Genet Año: 2021 Tipo del documento: Article País de afiliación: Finlandia Pais de publicación: Reino Unido

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