Transferrin mutations at the glycosylation site complicate diagnosis of congenital disorders of glycosylation type I
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Machiko Kadoya | Y. Wada | R. Wevers | L. P. Van den Heuvel | J. Zeman | E. Morava | D. Lefeber | I. Yuasa | H. Hansíková | N. Ondrušková | M. Guillard | K. Veselá | Alice Janssen