Literature DB >> 171873

[Transferrin variants: significance and identification in paternity cases (author's transl)].

G Mauff, E Doppelfeld, W Weber.   

Abstract

Transferrin phenotypes were determined in 3380 sera of unrelated persons of the western region of Germany with 97.60 percent for TfC and 2.40 percent for Tf variants. Identification was achieved by immunochemical means or through autoradiography. Relative mobilities in some variants were measured using Tf B2C (0.7) as reference. Application of Tf variants is demonstrated in paternity cases.

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Year:  1975        PMID： 171873

Source DB:  PubMed          Journal:  Z Immunitatsforsch Exp Klin Immunol        ISSN： 0300-872X


  4 in total

1.  [Experimental studies on population genetics of complement 3 (C3) and serum component transferin (Tf) in the population of Northern Bavaria].

Authors:  G Sittner; D Wiebecke; K Trenkel
Journal:  Blut       Date:  1976-06

2.  A third common allele in the transferrin system, TfC3, detected by isoelectric focusing.

Authors:  P Kühnl; W Spielmann
Journal:  Hum Genet       Date:  1979       Impact factor: 4.132

3.  Transferrin: evidence for two common subtypes of the TfC allele.

Authors:  P Kühnl; W Spielmann
Journal:  Hum Genet       Date:  1978-07-12       Impact factor: 4.132

4.  Isoelectric focusing of rare transferrin (Tf) variants and common TfC subtypes.

Authors:  P Kühnl; W Spielmann; W Weber
Journal:  Hum Genet       Date:  1979-01-19       Impact factor: 4.132
  4 in total

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