Congenital disorder of glycosylation (PMM2‐CDG) in a patient with antithrombin deficiency and severe thrombophilia

de la Morena‐Barrio ME, Sevivas TS, Martínez‐Martínez I, Miñano A, Vicente V, Jaeken J, Corral J. Congenital disorder of glycosylation (PMM2‐CDG) in a patient with antithrombin deficiency and severe thrombophilia. J Thromb Haemost 2012; 10: 2625–7.

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Bibliographic Details
Published in:Journal of thrombosis and haemostasis 2012-12, Vol.10 (12), p.2625-2627
Main Authors: DE LA MORENA‐BARRIO, M. E., SEVIVAS, T. S., MARTINEZ‐MARTINEZ, I., MIÑANO, A., VICENTE, V., JAEKEN, J., CORRAL, J.
Format: Article
Language:English
Subjects:
Adolescent
Antithrombins - metabolism
Congenital Disorders of Glycosylation - complications
Congenital Disorders of Glycosylation - diagnosis
Humans
Male
Thrombophilia - complications
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Summary:de la Morena‐Barrio ME, Sevivas TS, Martínez‐Martínez I, Miñano A, Vicente V, Jaeken J, Corral J. Congenital disorder of glycosylation (PMM2‐CDG) in a patient with antithrombin deficiency and severe thrombophilia. J Thromb Haemost 2012; 10: 2625–7.
ISSN:1538-7933
1538-7836
1538-7836
DOI:10.1111/jth.12031