Title : Glycophorin A in two patients with congenital dyserythropoietic anemia type I and type II is partly unglycosylated.

Pub. Date : 2000

PMID : 11310976






1 Functional Relationships(s)
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1 The results showed a large deficit of N-acetylgalactosamine, galactose, and sialic acid residues in glycophorin A from patients with CDA type I and type II amounting to about 45% and 55%, respectively. N-Acetylneuraminic Acid glycophorin A (MNS blood group) Homo sapiens