The HNF1A mutant Ala180Val: Clinical challenges in determining causality of a rare HNF1A variant in familial diabetes
| Autor: | Sagen, J.V., Bjørkhaug, L., Haukanes, B.I., Grevle, L., Molnes, J., Nedrebø, B.G., Søvik, O., Njølstad, P.R., Johansson, S., Molven, A. |
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| Zdroj: | In Diabetes Research and Clinical Practice November 2017 133:142-149 |
| Databáze: | ScienceDirect |
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