Subtypes of transferrin C

Human Heredity
H StiblerC Silkström

Abstract

Subtypes of transferrin C were studied by means of isoelectric focusing after complete desialylation of transferrin. Family data were consistent with an autosomal co-dominant mode of inheritance. Studies of serum samples from 75 individuals heterozygous for C and another (B or D) variant showed that the genes (C1 and C2) controlling the C subtypes are allelic to the B and D genes. The C2 gene frequency in Swedes and Swedish Lapps was similar to that found previously in Danes and Germans.

Citations

Oct 1, 1980·Italian Journal of Neurological Sciences·B RocchelliV Cosi
Jan 1, 1990·Archives of Disease in Childhood·H Stibler, J Jaeken
Jan 1, 1984·Critical Reviews in Clinical Laboratory Sciences·D D Dykes, H F Polesky
Apr 1, 1990·Forensic Science International : Synergy·K KishiW Sato
Jun 1, 1988·Alcoholism, Clinical and Experimental Research·U J BehrensC S Lieber
Jun 1, 1988·Alcoholism, Clinical and Experimental Research·H StiblerG Beckman
Oct 1, 1987·Alcoholism, Clinical and Experimental Research·H Stibler, R Hultcrantz
Mar 1, 1985·Jinrui idengaku zasshi. The Japanese journal of human genetics·I M SebetanS Akaishi
Mar 1, 1984·Italian Journal of Neurological Sciences·E MerelliP Bortolotti
Jan 1, 1980·Hereditas·G BeckmanC Sikström

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