de-la-Morena-Barrio, María-Eugenia; Sabater-Molina, María; de-la-Morena-Barrio, Belén; Ruhaak, Renee-L; Miñano, Antonia; Padilla, José; Toderici, Mara; Roldán-Schilling, Vanesa; Gimeno-Blanes, Juan-Ramón; Vicente, Vicente; Corral, Javier
(WILEY, 2020-08)
BACKGROUND: Congenital disorder of glycosylation (CDG) type I is a group of rare disorders caused by recessive mutations in up to 25 genes that impair the N-glycan precursor formation and its transfer to proteins resulting ...