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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
1979-12-20
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pubmed:abstractText |
The polymorphism of the properdin factor B (Bf, C3-proactivator, GBG = glycin-rich-beta-glycoprotein) has been investigated by high voltage agarose gel immunofixation electrophoresis in 1115 unrelated persons from Southern Germany. Seven phenotypes were observed; the allele frequencies were calculated as BfS = 0.8094, BfF = 0.1790, BfSI = 0.0094, BfFI = 0.0022. A study of 94 parents with 98 children and 420 mother-child combinations showed no deviation from the assumed autosomal codominant mode of inheritance. In one additional family the findings suggested the existence of a silent allele at the Bf-locus.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
0044-3433
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
83
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
259-64
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pubmed:dateRevised |
2008-2-20
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pubmed:meshHeading |
pubmed-meshheading:291240-Alleles,
pubmed-meshheading:291240-Complement Factor B,
pubmed-meshheading:291240-Electrophoresis, Agar Gel,
pubmed-meshheading:291240-Enzyme Precursors,
pubmed-meshheading:291240-Genetic Markers,
pubmed-meshheading:291240-Humans,
pubmed-meshheading:291240-Polymorphism, Genetic
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pubmed:year |
1979
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pubmed:articleTitle |
Properdin factor B-polymorphism. An indication for the existence of a Bf O-allele.
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pubmed:publicationType |
Journal Article
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