Deficiency of the first mannosylation step in the N-glycosylation pathway causes congenital disorder of glycosylation type Ik. (Q34288313)

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Deficiency of the first mannosylation step in the N-glycosylation pathway causes congenital disorder of glycosylation type Ik.
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    Deficiency of the first mannosylation step in the N-glycosylation pathway causes congenital disorder of glycosylation type Ik. (English)
    Claudia E Grubenmann
    Christian G Frank
    Andreas J Hülsmeier
    Els Schollen
    Gert Matthijs
    Ertan Mayatepek
    Thierry Hennet
    6 January 2004

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