| Literature DB >> 6567578 |
K Tokunaga, K Omoto, Y Yukiyama, M Sakurai, H Saji, E Maruya.
Abstract
A family was found which indicated the existence of a silent allele (BF*QO) at the locus for complement factor B. Three generations with eight members were studied. Four individuals were considered to be heterozygous for B deficiency because of unusual segregation patterns of the BF electrophoretic variants and low levels of B. Haplotype study on the other HLA-linked markers supported the presumption. No unusual products were detected by immunoblotting after sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE).Entities:
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Year: 1984 PMID: 6567578 DOI: 10.1007/bf00291408
Source DB: PubMed Journal: Hum Genet ISSN: 0340-6717 Impact factor: 4.132