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Dive into the research topics of 'MPDU1 mutations underlie a novel human congenital disorder of glycosylation, designated type If'. Together they form a unique fingerprint.- Sort by
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B. Schenk, T. Imbach, C. G. Frank, C. E. Grubenmann, G. V. Raymond, H. Hurvitz, A. Raas-Rotschild, A. S. Luder, J. Jaeken, E. G. Berger, G. Matthijs, T. Hennet, M. Aebi
Research output: Contribution to journal › Article › peer-review