A multigenerational study on phenotypic consequences of the most common causal variant of HNF1A-MODY.Published in:Diabetologia, 2022, v. 65, n. 4, p. 632, doi. 10.1007/s00125-021-05631-zBy:Kettunen, Jarno L. T.;Rantala, Elina;Dwivedi, Om P.;Isomaa, Bo;Sarelin, Leena;Kokko, Paula;Hakaste, Liisa;Miettinen, Päivi J.;Groop, Leif C.;Tuomi, TiinamaijaPublication type:Article