Erythrocyte Webb-type glycophorin C variant lacks N-glycosylation due to an asparagine to serine substitution.

Published

Journal Article

We have analyzed part of the sequence of the human glycophorin C (GPC) gene carried by a Webb blood-group positive donor. Our results indicate that the lack of N-glycosylation of the variant GPC associated with the Webb phenotype is due to a point mutation resulting in an asparagine to serine substitution at amino acid position 8.

Full Text

Duke Authors

Cited Authors

  • Telen, MJ; Le Van Kim, C; Guizzo, ML; Cartron, JP; Colin, Y

Published Date

  • May 1991

Published In

Volume / Issue

  • 37 / 1

Start / End Page

  • 51 - 52

PubMed ID

  • 1902622

Pubmed Central ID

  • 1902622

International Standard Serial Number (ISSN)

  • 0361-8609

Digital Object Identifier (DOI)

  • 10.1002/ajh.2830370112

Language

  • eng

Conference Location

  • United States