COG8 deficiency causes new congenital disorder of glycosylation type IIh.
Kranz, Christian; Ng, Bobby G.; Sun, Liangwu; Sharma, Vandana; Eklund, Erik A.; Miura, Yoshiaki; Ungar, Daniel; Lupashin, Vladimir; Winkel, R. Dennis; Cipollo, John F.; Costello, Catherine E.; Loh, Eva; Hong, Wanjin; Freeze, Hudson H.; Human Molecular Genetics, 2007, vol. 16, issue 7, p 731, ISSN 09646906. ISBN 09646906.

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