Assessing the relationship between monoallelic PRKN mutations and Parkinson's risk.

MLA

Lubbe, Steven J., et al. “Assessing the Relationship between Monoallelic PRKN Mutations and Parkinson’s Risk.” Human Molecular Genetics, vol. 30, no. 1, Jan. 2021, pp. 78–86. EBSCOhost, https://doi.org/10.1093/hmg/ddaa273.

APA

Lubbe, S. J., Bustos, B. I., Hu, J., Krainc, D., Joseph, T., Hehir, J., Tan, M., Zhang, W., Escott-Price, V., Williams, N. M., Blauwendraat, C., Singleton, A. B., Morris, H. R., & IPDGC), for International Parkinson’s Disease Genomics Consortium. (2021). Assessing the relationship between monoallelic PRKN mutations and Parkinson’s risk. Human Molecular Genetics, 30(1), 78–86. https://doi.org/10.1093/hmg/ddaa273

Chicago

Lubbe, Steven J, Bernabe I Bustos, Jing Hu, Dimitri Krainc, Theresita Joseph, Jason Hehir, Manuela Tan, et al. 2021. “Assessing the Relationship between Monoallelic PRKN Mutations and Parkinson’s Risk.” Human Molecular Genetics 30 (1): 78–86. doi:10.1093/hmg/ddaa273.