A multigenerational study on phenotypic consequences of the most common causal variant of HNF1A-MODY

AIMS/HYPOTHESIS: Systematic studies on the phenotypic consequences of variants causal of HNF1A-MODY are rare. Our aim was to assess the phenotype of carriers of a single HNF1A variant and genetic and clinical factors affecting the clinical spectrum. METHODS: We conducted a family-based multigenerati...

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Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8894160/
https://www.ncbi.nlm.nih.gov/pubmed/34951657
http://dx.doi.org/10.1007/s00125-021-05631-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8894160/
https://www.ncbi.nlm.nih.gov/pubmed/34951657
http://dx.doi.org/10.1007/s00125-021-05631-z

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