Analysis of FMO3 gene variants in Argentine patients: Implications for the diagnosis of Trimethylaminuria.

por Silvera Ruiz, SM, Grosso, CL, Castro, GM, Dodelson de Kremer, R, Angaroni , CJ
Publicado 2023

Urea Cycle defects in Argentina. Rare or undiagnosed diseases? Local experience in its diagnosis and characterization

por Silvera Ruiz , SM, Angaroni, CJ, Grosso, CL, Guelbert, N, Becerra, A, Peralta , F, Dodelson de Kremer, R, Laróvere, LE
Publicado 2019