Cita APA

S, P., A, M., B, D., M, T., J, M., R, M., . . . ABP, v. K. (2019). Deficiency of perforin and hCNT1, a novel inborn error of pyrimidine metabolism, associated with a rapidly developing lethal phenotype due to multi-organ failure.

Citación estilo Chicago

S, Pérez-Torras, et al. Deficiency of Perforin and HCNT1, a Novel Inborn Error of Pyrimidine Metabolism, Associated With a Rapidly Developing Lethal Phenotype Due to Multi-organ Failure. 2019.

Cita MLA

S, Pérez-Torras, et al. Deficiency of Perforin and HCNT1, a Novel Inborn Error of Pyrimidine Metabolism, Associated With a Rapidly Developing Lethal Phenotype Due to Multi-organ Failure. 2019.