Literature DB >> 489033

Subtypes of transferrin C.

H Stibler, G Beckman, C 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.

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Year:  1979        PMID： 489033     DOI： 10.1159/000153065

Source DB:  PubMed          Journal:  Hum Hered        ISSN： 0001-5652            Impact factor:   0.444


  6 in total

1.  Transferrin protein variant mimicking carbohydrate-deficient glycoprotein syndrome in trisomy 7 mosaicism.

Authors:  C Knopf; R Rod; J Jaeken; M Berant; E Van Schaftingen; J P Fryns; R Brill-Zamir; R Gershoni-Baruch; S Lischinsky; H Mandel
Journal:  J Inherit Metab Dis       Date:  2000-06       Impact factor: 4.982

2.  Genetic polymorphism of the B subunit of human coagulation factor XIII: another classification.

Authors:  Y Kera; H Nishimukai; K Yamasawa
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

3.  Transferrin (Tf) subtyping on agarose: a new technique for isoelectric focusing.

Authors:  D Dykes; H Polesky
Journal:  Hum Genet       Date:  1981       Impact factor: 4.132

4.  A new procedure for the determination of transferrin C (Tf C) subtypes by isoelectric focusing. Existence of two additional alleles, Tf C4 and Tf C5.

Authors:  J Constans; P Kühnl; M Viau; W Spielmann
Journal:  Hum Genet       Date:  1980       Impact factor: 4.132

5.  Isoelectric focusing with immobilized pH gradients for the analysis of transferrin (Tf) subtypes and variants.

Authors:  A Görg; J Weser; R Westermeier; W Postel; S Weidinger; W Patutschnick; H Cleve
Journal:  Hum Genet       Date:  1983       Impact factor: 4.132

6.  Carbohydrate deficient serum transferrin in a new systemic hereditary syndrome.

Authors:  H Stibler; J Jaeken
Journal:  Arch Dis Child       Date:  1990-01       Impact factor: 3.791
  6 in total

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