Genetic complementation reveals a novel human congenital disorder of glycosylation of type II, due to inactivation of the Golgi CMP-sialic acid transporter

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https://hal.archives-ouvertes.fr/hal-00088624
Contributor : Isabelle Frapart <>
Submitted on : Thursday, August 3, 2006 - 3:41:46 PM
Last modification on : Wednesday, June 27, 2018 - 8:24:02 AM

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I. Martinez-Duncker, T. Dupré, V. Piller, F. Piller, J.J. Candelier, et al.. Genetic complementation reveals a novel human congenital disorder of glycosylation of type II, due to inactivation of the Golgi CMP-sialic acid transporter. Blood, American Society of Hematology, 2005, 105, pp.2671-2676. ⟨hal-00088624⟩

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