Deficiency of the first mannosylation step in the N-glycosylation pathway causes congenital disorder of glycosylation type Ik. (Q34288313)
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English | 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)
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Markus Aebi
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Eric G Berger
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Claudia E Grubenmann
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Christian G Frank
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Andreas J Hülsmeier
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Els Schollen
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Gert Matthijs
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Ertan Mayatepek
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Thierry Hennet
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6 January 2004
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