Reisz, J.A.; Dzieciatkowska, M.; Stephenson, D.; Gamboni, F.; Morton, D.H.; 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, 1699.
https://doi.org/10.3390/antiox12091699
AMA Style
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
Chicago/Turabian Style
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
APA Style
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
