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Transferrin mutations at the glycosylation site complicate d…
Transferrin mutations at the glycosylation site complicate diagnosis of congenital disorders of glycosylation type I
Transferrin mutations at the glycosylation site complicate diagnosis of congenital disorders of glycosylation type I
Article, Chapter
Authors: M. Guillard
Publication: Journal of Inherited Metabolic Disease, Volume:34, Issue:4, Page(s):901-906
Published: Springer Netherlands, 2011
ISSN: 0141-8955
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