Congenital disorder of glycosylation type Id (CDG Id) : phenotypic, biochemical and molecular characterization of a new patient
Rimella-Le-Huu A., 2010. 13, Université de Lausanne, Faculté de biologie et médecine, Bonafé L. (dir.).
Congenital disorder of glycosylation type Id (CDG Id) : phenotypic, biochemical and molecular characterization of a new patient
Rimella-Le-Huu A., 2010. 13, Université de Lausanne, Faculté de biologie et médecine, Bonafé L. (dir.).
Congenital disorder of glycosylation type Id (CDG Id): phenotypic, biochemical and molecular characterization of a new patient.
Rimella-Le-Huu A., Henry H., Kern I., Hanquinet S., Roulet-Perez E., Newman C.J., Superti-Furga A., Bonafé L., Ballhausen D., 2008. Journal of Inherited Metabolic Disease. Peer-reviewed.
Congenital disorder of glycosylation type Id (CDG Id): phenotypic, biochemical and molecular characterization of a new patient.
Rimella-Le-Huu A., Henry H., Kern I., Hanquinet S., Roulet-Perez E., Newman C.J., Superti-Furga A., Bonafé L., Ballhausen D., 2008. Journal of Inherited Metabolic Disease. Peer-reviewed.