COG8 deficiency causes new congenital disorder of glycosylation type IIh.
Kranz C; Ng BG; Sun L; Sharma V; Eklund EA; Miura Y; Ungar D; Lupashin V; Winkel RD; Cipollo JF; Costello CE; Loh E; Hong W; Freeze HH; Human Molecular Genetics, 2007, vol. 16, issue 7, p 731, ISSN 09646906. ISBN 09646906.

Full Text Resources Located for this Citation

View article on EBSCOhost(Login required)
View article via CrossRef