APA

Vuillaumier-Barrot S., Hetet G., Barnier A., Dupré T., Cuer M., de Lonlay P., Cormier-Daire V., Durand G., Grandchamp B. & Seta N. (20000912). Identification of four novel PMM2 mutations in congenital disorders of glycosylation (CDG) Ia French patients. : Journal of medical genetics.

Chicago

Vuillaumier-Barrot S, Hetet G, Barnier A, Dupré T, Cuer M, de Lonlay P, Cormier-Daire V, Durand G, Grandchamp B and Seta N. 20000912. Identification of four novel PMM2 mutations in congenital disorders of glycosylation (CDG) Ia French patients. : Journal of medical genetics.

Harvard

Vuillaumier-Barrot S., Hetet G., Barnier A., Dupré T., Cuer M., de Lonlay P., Cormier-Daire V., Durand G., Grandchamp B. and Seta N. (20000912). Identification of four novel PMM2 mutations in congenital disorders of glycosylation (CDG) Ia French patients. : Journal of medical genetics.

MLA

Vuillaumier-Barrot S, Hetet G, Barnier A, Dupré T, Cuer M, de Lonlay P, Cormier-Daire V, Durand G, Grandchamp B and Seta N. Identification of four novel PMM2 mutations in congenital disorders of glycosylation (CDG) Ia French patients. : Journal of medical genetics. 20000912.