Variation of the serum N ‐glycosylation during the pregnancy of a MPI‐CDG patient-Reference-Cited by-同舟云学术

Variation of the serum N ‐glycosylation during the pregnancy of a MPI‐CDG patient

Published:2021-09-17 Issue:1 Volume:62 Page:22-29
ISSN:2192-8312
Container-title:JIMD Reports
language:en
Short-container-title:JIMD Reports

Author:

Lebredonchel Elodie¹²^ORCID,Duvet Sandrine¹,Douillard Claire³,Foulquier François¹,Klein André¹²

Affiliation:

1. UGSF—Unité de Glycobiologie Structurale et Fonctionnelle, UMR 8576 Université de Lille, CNRS Lille France

2. Pôle Biologie Pathologie Génétique, Institut de Biochimie et de Biologie Moléculaire, UAM de Glycopathologies Université de Lille, CHU Lille Lille France

3. Centre de Référence des Maladies Héréditaires du Métabolisme, Hôpital Huriez CHU de Lille, Département d'Endocrinologie et Métabolisme Lille France

Publisher

Wiley

Subject

Biochemistry, Genetics and Molecular Biology (miscellaneous),Endocrinology, Diabetes and Metabolism,Internal Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jmd2.12247

Reference38 articles.

1. Familial psychomotor retardation with markedly fluctuating serum prolactin, FSH and GH levels, partial TBG-deficiency, increased serum arylsulphatase A and increased CSF protein: a new syndrome?: 90

2. Congenital disorders of glycosylation: a multi‐genetic disease family with multiple subcellular locations;Jaeken J;J Mother Child,2020

3. Carbohydrate-deficient glycoprotein syndrome type Ib. Phosphomannose isomerase deficiency and mannose therapy.

4. The Metabolic Origins of Mannose in Glycoproteins

5. Gastrointestinal and Other Clinical Manifestations in 17 Children With Congenital Disorders of Glycosylation Type Ia, Ib, and Ic

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