Identification of four novel PMM2 mutations in congenital disorders of glycosylation (CDG) Ia French patients

Por Vuillaumier-Barro..., S., Hetet, G., Barnier, A., Dupre, T., Cuer, M., de Lonlay, P., Cormier-Daire, V., Durand, G., Grandchamp, B., Seta, N.
Publicado em 2000

Idiopathic dilated cardiomyopathy: lack of association with haemochromatosis gene in the CARDIGENE study

Por HETET, G, GRANDCHAMP, B, BOUCHIER, C, NICAUD, V, TIRET, L, ROIZES, G, DESNOS, M, SCHWARTZ, K, DORENT, R, KOMAJDA, M, GROUP, F. T.
Publicado em 2001