(Q24675360)
Statements
Clinical and molecular features of three patients with congenital disorders of glycosylation type Ih (CDG-Ih) (ALG8 deficiency) (English)
E Schollen
C G Frank
L Keldermans
R Reyntjens
C E Grubenmann
P T Clayton
B G Winchester
J Smeitink
M Aebi
T Hennet