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Number of results
2009 | 50 | 2 | 149-152

Article title

Identification of carriers of the mutation causing coagulation factor XI deficiency in Polish Holstein-Friesian cattle

Title variants

Languages of publication

EN

Abstracts

EN
Factor XI (FXI) deficiency is a hereditary coagulation disorder observed in various mammalian species. The molecular basis of coagulopathy has been recognized in Holstein cattle as a 76-bp insertion in the coding region of the FXI gene. Because the disorder seems to have an impact on reproductive traits and udder health in cattle, we tested 103 randomly selected cows, 28 cows with repeat breeding, and 9 cows with recurrent mastitis for the presence of an abnormal FXI allele. Three related cows were diagnosed as carriers.

Discipline

Year

Volume

50

Issue

2

Pages

149-152

Physical description

Contributors

author
author
author

References

Document Type

ARTICLE

Publication order reference

A. Gurgul, Department of Animal Immuno- and Cytogenetics, National Research Institute of Animal Production, Krakowska 1, 32-083 Balice, Poland

Identifiers

YADDA identifier

bwmeta1.element.element-from-psjc-ce97088d-4d81-3f5a-922e-62f8d0a7bbc3
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