Citations refer to the original publication, not to a Scieee localized version.
Johansson, E., Kallionpää, R. A., Böckerman, P., Peltonen, S., & Peltonen, J. (2022). The rare disease neurofibromatosis 1 as a source of hereditary economic inequality : evidence from Finland. Genetics in Medicine, (4). https://jyx.jyu.fi/handle/123456789/85631
Johansson, Edvard, et al. “The rare disease neurofibromatosis 1 as a source of hereditary economic inequality : evidence from Finland.” Genetics in Medicine, no. 4, 2022. https://jyx.jyu.fi/handle/123456789/85631.
Johansson, Edvard, Roope A. Kallionpää, Petri Böckerman, Sirkku Peltonen, and Juha Peltonen. “The rare disease neurofibromatosis 1 as a source of hereditary economic inequality : evidence from Finland.” Genetics in Medicine, no. 4 (2022). https://jyx.jyu.fi/handle/123456789/85631.
Johansson, E. et al. (2022) ‘The rare disease neurofibromatosis 1 as a source of hereditary economic inequality : evidence from Finland’, Genetics in Medicine, (4). Available at: https://jyx.jyu.fi/handle/123456789/85631.
E. Johansson, R. A. Kallionpää, P. Böckerman, S. Peltonen, and J. Peltonen, “The rare disease neurofibromatosis 1 as a source of hereditary economic inequality : evidence from Finland,” Genetics in Medicine, no. 4, 2022. [Online]. Available: https://jyx.jyu.fi/handle/123456789/85631
@article{johansson2022rare,
author = {Johansson, Edvard and Kallionpää, Roope A. and Böckerman, Petri and Peltonen, Sirkku and Peltonen, Juha},
title = {The rare disease neurofibromatosis 1 as a source of hereditary economic inequality : evidence from Finland},
journal = {Genetics in Medicine},
year = {2022},
number = {4},
publisher = {Elsevier},
url = {https://jyx.jyu.fi/handle/123456789/85631}
}
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