Factor XIII Deficiency
- 1 January 1979
- journal article
- research article
- Published by S. Karger AG in Acta Haematologica
- Vol. 62 (3) , 167-172
- https://doi.org/10.1159/000207564
Abstract
A girl with congenital factor XIII deficiency and her large family have been studied by electroimmunoassay of factor XIII subunits A and S. The homozygote has absence of subunit A and a decreased level of subunit S. The heterozygotes have decreased levels of both subunits, and were more readily identified by measurement of subunit A than by the ratio subunit S/subunit A. The mother of the propositus appears to be a new heterozygote, but heterozygosity on the paternal side is traced through three generations.Keywords
This publication has 2 references indexed in Scilit:
- Subunits A and S Inheritance in Four Families with Congenital Factor XIII DeficiencyBritish Journal of Haematology, 1978
- Quantitative estimation of proteins by electrophoresis in agarose gel containing antibodiesAnalytical Biochemistry, 1966