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

Ivan Martinez-Duncker; Thierry Dupré; Véronique Piller; Friedrich Piller; Jean-Jacques Candelier; Catherine Trichet; Gil Tchernia; Rafael Oriol; Rosella Mollicone

doi:10.1182/blood-2004-09-3509

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

Identifier:nobleid.org/w1/20260515/C189CD98

Type:Journal Article

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Ivan Martinez-Duncker

Thierry Dupré

Véronique Piller

Friedrich Piller

Jean-Jacques Candelier

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

Identifier:nobleid.org/w1/20260515/C189CD98

Type:Journal Article

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[![NobleID](https://www.nobleid.org/api/badge/C189CD98.svg?ark=w1%2F20260515%2FC189CD98)](https://nobleid.org/work/w1/20260515/C189CD98)

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Paper Authors

Ivan Martinez-Duncker

Thierry Dupré

Véronique Piller

Friedrich Piller

Jean-Jacques Candelier

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