Search Results - Kienz, Petra

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  1. 1
    A mutation in the human MPDU1 gene causes congenital disorder of glycosylation type If (CDG-If)

    A mutation in the human MPDU1 gene causes congenital disorder of glycosylation type If (CDG-If) by Kranz, C, Denecke, J, Lehrman, M A, Ray, S, Kienz, P, Kreissel, G, Sagi, D, Peter-Katalinic, J, Freeze, H H, Schmid, T, Jackowski-Dohrmann, S, Harms, E, Marquardt, T

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  2. 2
    Glycoproteomics of N-glycosylation by in-gel deglycosylation and matrix-assisted laser desorption/ionisation-time of flight mass spectrometry mapping: Application to congenital disorders of glycosylation

    Glycoproteomics of N-glycosylation by in-gel deglycosylation and matrix-assisted laser desorption/ionisation-time of flight mass spectrometry mapping: Application to congenital dis... by Šagi, Dijana, Kienz, Petra, Denecke, Jonas, Marquardt, Thorsten, Peter-Katalinić, Jasna

    Published in Proteomics (Weinheim)
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