Capillary zone electrophoresis of transferrin and EDTA samples in congenital disorders of glycosylation screening: CaNOt do, really?

Clin Chim Acta. 2021 Aug:519:92-93. doi: 10.1016/j.cca.2021.04.013. Epub 2021 Apr 20.

Authors

Alexandre Raynor¹, Célia Raulet-Bussian¹, Léa Verel¹, Grégory Plouviez¹, Arnaud Bruneel²

Affiliations

¹ AP-HP, Biochimie Métabolique et Cellulaire, Hôpital Bichat-Claude Bernard, Paris, France.
² AP-HP, Biochimie Métabolique et Cellulaire, Hôpital Bichat-Claude Bernard, Paris, France. Electronic address: arnaud.bruneel@aphp.fr.

PMID: 33891959
DOI: 10.1016/j.cca.2021.04.013

No abstract available

Publication types

Letter

MeSH terms

Congenital Disorders of Glycosylation* / diagnosis
Congenital Disorders of Glycosylation* / genetics
Edetic Acid
Electrophoresis, Capillary
Humans
Isoelectric Focusing
Transferrin*

Substances

Transferrin
Edetic Acid