Kytövuori, L., Sipilä, J., Doi, H., Hurme-Niiranen, A., Siitonen, A., Koshimizu, E., . . . Majamaa, K. (2022). Biallelic expansion in RFC1 as a rare cause of Parkinson’s disease. Nature Portfolio.
Chicago Style (17th ed.) CitationKytövuori, Laura, et al. Biallelic Expansion in RFC1 as a Rare Cause of Parkinson’s Disease. Nature Portfolio, 2022.
MLA (9th ed.) CitationKytövuori, Laura, et al. Biallelic Expansion in RFC1 as a Rare Cause of Parkinson’s Disease. Nature Portfolio, 2022.
Warning: These citations may not always be 100% accurate.