MPDU1 mutations underlie a novel human congenital disorder of glycosylation, designated type If.
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G. Raymond | E. Berger | T. Hennet | M. Aebi | A. Luder | G. Matthijs | J. Jaeken | I. Korn‐Lubetzki | H. Hurvitz | C. Frank | A. Raas-Rotschild | T. Imbach | B. Schenk | C. Grubenmann | S. Revel-Vik