A newborn Screening Programme for Inborn errors of metabolism in Galicia: 22 years of evaluation and follow-up.

Autor: Couce, María L.1,2 (AUTHOR) maria.luz.couce.pico@sergas.es, Bóveda, María-Dolores1,2 (AUTHOR), Castiñeiras, Daisy E.1,2 (AUTHOR), Vázquez-Mosquera, María-Eugenia1,2 (AUTHOR), Barbosa-Gouveia, Sofía1,2 (AUTHOR), De Castro, María-José1,2 (AUTHOR), Iglesias-Rodríguez, Agustin J.1,2 (AUTHOR), Colón, Cristóbal1,2 (AUTHOR), Cocho, José A.1,2 (AUTHOR), Sánchez, Paula1,2 (AUTHOR)
Zdroj: Orphanet Journal of Rare Diseases. 5/17/2024, Vol. 19 Issue 1, p1-11. 11p.
Databáze: Academic Search Ultimate
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