PubMed · 1975 · 59 citations · 47 references
Life SciencesBiochemistryGeneticsBiochemical GeneticsHuman GeneticsMedical GeneticsFamily-based Genetic AnalysisBiological Paternity ClaimsC-type Lectin Receptor PolymorphismsPaternity ProceedingsProperdin Deficiency
Determination of genetic properdin factor B(Bf) polymorphism was carried out in immunofixation electrophoresis. Genetics of factor B were also studied after ageing, conversion with cobra venom and neuraminidase. In population studies the distribution of factor B in a West German population of 1245 non-related individuals was found to be: Bf F 2.73%, Bf FS 28.43%, Bf S 65.38%. Rare phenotypes (F 1F,F 1S, FS 1, SS 1) were seen in 3.46%. In addition a new variant, designated F1.6S, was observed. The application of factor B polymorphism to 68 paternity cases is discussed.
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