[Transferrin Variants: Significance and Identification in Paternity Cases (author's Transl)]

Overview

Journal Z Immunitatsforsch Exp Klin Immunol

Specialties Allergy & Immunology
Microbiology

Date 1975 Aug 1

PMID 171873

Citations 4

Authors

G Mauff

E Doppelfeld

W Weber

Affiliations

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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.

Citing Articles

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

Sittner G, Wiebecke D, Trenkel K Blut. 1976; 32(6):447-50.

PMID: 1276485 DOI: 10.1007/BF01013886.

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

Kuhnl P, SPIELMANN W Hum Genet. 1978; 43(1):91-5.

PMID: 669722 DOI: 10.1007/BF00396483.

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

Kuhnl P, SPIELMANN W Hum Genet. 1979; 50(2):193-8.

PMID: 511134 DOI: 10.1007/BF00390241.

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

Kuhnl P, SPIELMANN W, Weber W Hum Genet. 1979; 46(1):83-7.

PMID: 429010 DOI: 10.1007/BF00278905.