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Reisz JA, Dzieciatkowska M, Stephenson D, Gamboni F, Morton DH, D’Alessandro A. Red Blood Cells from Individuals with Lesch–Nyhan Syndrome: Multi-Omics Insights into a Novel S162N Mutation Causing Hypoxanthine-Guanine Phosphoribosyltransferase Deficiency. Antioxidants. 2023; 12(9):1699. https://doi.org/10.3390/antiox12091699

Reisz, Julie A., Monika Dzieciatkowska, Daniel Stephenson, Fabia Gamboni, D. Holmes Morton, and Angelo D’Alessandro. 2023. "Red Blood Cells from Individuals with Lesch–Nyhan Syndrome: Multi-Omics Insights into a Novel S162N Mutation Causing Hypoxanthine-Guanine Phosphoribosyltransferase Deficiency" Antioxidants 12, no. 9: 1699. https://doi.org/10.3390/antiox12091699

Reisz, J. A., Dzieciatkowska, M., Stephenson, D., Gamboni, F., Morton, D. H., & D’Alessandro, A. (2023). Red Blood Cells from Individuals with Lesch–Nyhan Syndrome: Multi-Omics Insights into a Novel S162N Mutation Causing Hypoxanthine-Guanine Phosphoribosyltransferase Deficiency. Antioxidants, 12(9), 1699. https://doi.org/10.3390/antiox12091699