Cita APA (7a ed.)

Silvera Ruíz, S. M., Arranz Amo, A., Dodelson de Kremer, R., & Larovere, L. E. (2022). Ornithine transcarbamylase deficiency: Identification of mutations, computational validation, and phenotypic correlation in argentinian patients.

Cita Chicago Style (17a ed.)

Silvera Ruíz, Silene Maite, Antonio Arranz Amo, Raquel Dodelson de Kremer, y Laura Elena Larovere. Ornithine Transcarbamylase Deficiency: Identification of Mutations, Computational Validation, and Phenotypic Correlation in Argentinian Patients. 2022.

Cita MLA (8a ed.)

Silvera Ruíz, Silene Maite, et al. Ornithine Transcarbamylase Deficiency: Identification of Mutations, Computational Validation, and Phenotypic Correlation in Argentinian Patients. 2022.