Early Diagnosis and Treatment of Purine Nucleoside Phosphorylase (PNP) Deficiency through TREC-Based Newborn Screening

MLA

Andrea Martín-Nalda, et al. “Early Diagnosis and Treatment of Purine Nucleoside Phosphorylase (PNP) Deficiency through TREC-Based Newborn Screening.” International Journal of Neonatal Screening, vol. 7, no. 4, Sept. 2021, p. 62. EBSCOhost, https://doi.org/10.3390/ijns7040062.

APA

Andrea Martín-Nalda, Jacques G. Rivière, Mireia Català-Besa, Marina García-Prat, Alba Parra-Martínez, Mónica Martínez-Gallo, Roger Colobran, Ana Argudo-Ramírez, Jose Luis Marín-Soria, Judit García-Villoria, Laura Alonso, Jose Antonio Arranz-Amo, Giancarlo la Marca, & Pere Soler-Palacín. (2021). Early Diagnosis and Treatment of Purine Nucleoside Phosphorylase (PNP) Deficiency through TREC-Based Newborn Screening. International Journal of Neonatal Screening, 7(4), 62. https://doi.org/10.3390/ijns7040062

Chicago

Andrea Martín-Nalda, Jacques G. Rivière, Mireia Català-Besa, Marina García-Prat, Alba Parra-Martínez, Mónica Martínez-Gallo, Roger Colobran, et al. 2021. “Early Diagnosis and Treatment of Purine Nucleoside Phosphorylase (PNP) Deficiency through TREC-Based Newborn Screening.” International Journal of Neonatal Screening 7 (4): 62. doi:10.3390/ijns7040062.