The g277s mutation in transferrin does not disturb function
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2141.2003.04347.x/fullpdf
Reference3 articles.
1. Human transferrin G277S mutation: a risk factor for iron deficiency anaemia;Lee;British Journal of Haematology,2001
2. Expression of glycosylated and nonglycosylated human transferrin in mammalian cells. Characterization of the recombinant proteins with comparison to three commercially available transferrins;Mason;Biochemistry,1993
3. A kinetically active site in the C-lobe of human transferrin;Zak;Biochemistry,1997
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