Clinical and molecular features of three patients with congenital disorders of glycosylation type Ih (CDG-Ih) (ALG8 deficiency). Issue 7 (2nd July 2004) - Schollen, E; Frank, C G; Keldermans, L; Reyntjens, R; Grubenmann, C E; Clayton, P T; Winchester, B G; Smeitink, J; Wevers, R A; Aebi, M; Hennet, T; Matthijs, G