Zárybnický, T.; Heikkinen, A.; Kangas, S.M.; Karikoski, M.; MartÃnez-Nieto, G.A.; Salo, M.H.; Uusimaa, J.; Vuolteenaho, R.; Hinttala, R.; Sipilä, P.;
et al. Modeling Rare Human Disorders in Mice: The Finnish Disease Heritage. Cells 2021, 10, 3158.
https://doi.org/10.3390/cells10113158
AMA Style
Zárybnický T, Heikkinen A, Kangas SM, Karikoski M, MartÃnez-Nieto GA, Salo MH, Uusimaa J, Vuolteenaho R, Hinttala R, Sipilä P,
et al. Modeling Rare Human Disorders in Mice: The Finnish Disease Heritage. Cells. 2021; 10(11):3158.
https://doi.org/10.3390/cells10113158
Chicago/Turabian Style
Zárybnický, Tomáš, Anne Heikkinen, Salla M. Kangas, Marika Karikoski, Guillermo Antonio MartÃnez-Nieto, Miia H. Salo, Johanna Uusimaa, Reetta Vuolteenaho, Reetta Hinttala, Petra Sipilä,
and et al. 2021. "Modeling Rare Human Disorders in Mice: The Finnish Disease Heritage" Cells 10, no. 11: 3158.
https://doi.org/10.3390/cells10113158
APA Style
Zárybnický, T., Heikkinen, A., Kangas, S. M., Karikoski, M., MartÃnez-Nieto, G. A., Salo, M. H., Uusimaa, J., Vuolteenaho, R., Hinttala, R., Sipilä, P., & Kuure, S.
(2021). Modeling Rare Human Disorders in Mice: The Finnish Disease Heritage. Cells, 10(11), 3158.
https://doi.org/10.3390/cells10113158
