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Dive into the research topics of 'No overall hyposialylation in hereditary inclusion body myopathy myoblasts carrying the homozygous M712T GNE mutation'. Together they form a unique fingerprint.- Sort by
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Ilan Salama, Stephan Hinderlich, Zipora Shlomai, Iris Eisenberg, Sabine Krause, Kevin Yarema, Zohar Argov, Hanns Lochmuller, Werner Reutter, Ron Dabby, Menachem Sadeh, Hannah Ben-Bassat, Stella Mitrani-Rosenbaum
Research output: Contribution to journal › Article › peer-review