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Phosphomannomutase deficiency is the main cause of carbohydr…

Phosphomannomutase deficiency is the main cause of carbohydrate deficient glycoprotein syndrome with type I isoelectrofocusing pattern of serum sialotransferrins

Article, Chapter

Authors: J. Jaeken

Publication: Journal of Inherited Metabolic Disease, Volume:20, Issue:3, Page(s):447-449

Published: Springer Netherlands, 1997

ISSN: 0141-8955

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View Full Text Source:Journal of Inherited Metabolic Disease,Journal of Inherited Metabolic Disease,Springer Complete Journals Opens in new Window

Journal: Journal of Inherited Metabolic Disease Source:Springer Complete Journals Opens in new Window

Collection: Springer Complete Journals Opens in new Window

Coverage:

1978-03-01~2018-11-01; volume:1;issue:1~volume:41;issue:6

View Full Text Source:Journal of Inherited Metabolic Disease,Journal of Inherited Metabolic Disease,Wiley Online Library: Complete Journals Opens in new Window

Journal: Journal of Inherited Metabolic Disease Source:Wiley Online Library: Complete Journals Opens in new Window

Collection: Wiley Online Library: Complete Journals Opens in new Window

Coverage:

1997-02-01~present; volume:20~present

View Full Text Source:Journal of Inherited Metabolic Disease,Journal of Inherited Metabolic Disease,Wiley Online Library Database Model 2021 Opens in new Window

Journal: Journal of Inherited Metabolic Disease Source:Wiley Online Library Database Model 2021 Opens in new Window

Collection: Wiley Online Library Database Model 2021 Opens in new Window

Coverage:

1997~present; volume:20~present;issue:1~present

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