Opening book details…
About this Biochemistry, Genetics and Molecular Biology article
Transferrin mutations at the glycosylation site complicate diagnosis of congenital disorders of glycosylation type I by 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 is a Biochemistry, Genetics and Molecular Biology article available to read on EtoBox.
It is typically read by researchers, students, and practitioners in Biochemistry, Genetics and Molecular Biology.
- Author
- 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
- Publisher
- Springer; Wiley (John Wiley & Sons); Kluwer Academic Publishers; Wiley; Springer Science and Business Media LLC (ISSN 0141-8955)
- Published
- 2011
- Field
- Biochemistry, Genetics and Molecular Biology (Life Sciences)