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Article

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

Journal of applied genetics - 1 Jan 2009

Gurgul A, Rubis D, Slota E

Abstract excerpt

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...

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PMID: 19433912
DOI: 10.1007/BF03195666

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

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Identification of carriers of the mutation causing coagulation factor XI deficiency in Polish Holstein-Friesian cattle.PMID 19433912Read ↗

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