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Transferrin mutations at the glycosylation site complicate diagnosis of congenital disorders of glycosylation type i
Mailys Guillard, Yoshinao Wada, Hana Hansikova, Isao Yuasa, Katerina Vesela, Nina Ondruskova, MacHiko Kadoya, Alice Janssen, Lambertus P.W.J. Van Den Heuvel, Eva Morava, Jiri Zeman, Ron A. Wevers, Dirk J. Lefeber
Research output: Contribution to journal › Article › peer-review
24
Scopus
citations