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Dive into the research topics of 'A mutation in the human MPDU1 gene causes congenital disorder of glycosylation type If (CDG-If)'. Together they form a unique fingerprint.- Sort by
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C. Kranz, J. Denecke, M. A. Lehrman, S. Ray, P. Kienz, G. Kreissel, D. Sagi, J. Peter-Katalinic, H. H. Freeze, T. Schmid, S. Jackowski-Dohrmann, E. Harms, T. Marquardt
Research output: Contribution to journal › Article › peer-review