Ingvild Aukrust
0000-0002-4379-5654
3 papers found
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Characterisation of HNF1A variants in paediatric diabetes in Norway using functional and clinical investigations to unmask phenotype and monogenic diabetes
The contribution of functional HNF1A variants and polygenic susceptibility to risk of type 2 diabetes in ancestrally diverse populations
Functional Analyses of HNF1A-MODY Variants Refine the Interpretation of Identified Sequence Variants
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