Works matching IS 09646906 AND DT 2007 AND VI 16 AND IP 7


Results: 12
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    COG8 deficiency causes new congenital disorder of glycosylation type IIh.

    Published in:
    Human Molecular Genetics, 2007, v. 16, n. 7, p. 731, doi. 10.1093/hmg/ddm028
    By:
    • 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.
    Publication type:
    Article
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