APA

Rimella-Le-Huu A., Henry H., Kern I., Hanquinet S., Roulet-Perez E., Newman C. J., Superti-Furga A., Bonafé L. & Ballhausen D. (20120111). Congenital disorder of glycosylation type Id (CDG Id): phenotypic, biochemical and molecular characterization of a new patient. : Journal of inherited metabolic disease.

Chicago

Rimella-Le-Huu A, Henry H, Kern I, Hanquinet S, Roulet-Perez E, Newman C J, Superti-Furga A, Bonafé L and Ballhausen D. 20120111. Congenital disorder of glycosylation type Id (CDG Id): phenotypic, biochemical and molecular characterization of a new patient. : Journal of inherited metabolic disease.

Harvard

Rimella-Le-Huu A., Henry H., Kern I., Hanquinet S., Roulet-Perez E., Newman C. J., Superti-Furga A., Bonafé L. and Ballhausen D. (20120111). Congenital disorder of glycosylation type Id (CDG Id): phenotypic, biochemical and molecular characterization of a new patient. : Journal of inherited metabolic disease.

MLA

Rimella-Le-Huu A, Henry H, Kern I, Hanquinet S, Roulet-Perez E, Newman C J, Superti-Furga A, Bonafé L and Ballhausen D. Congenital disorder of glycosylation type Id (CDG Id): phenotypic, biochemical and molecular characterization of a new patient. : Journal of inherited metabolic disease. 20120111.