A classification system for cross-reactive material-negative factor XI deficiency

The bleeding disorder associated with factor XI (fXI) deficiency is typically inherited as an autosomal recessive trait. However, some fXI mutations may be associated with dominant disease transmission. FXI is a homodimer, a feature that could allow certain mutations to exert a dominant-negative eff...

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Bibliografiske detaljer
Main Authors: Kravtsov, Dmitri V., Monahan, Paul E., Gailani, David
Format: Artigo
Sprog:Inglês
Udgivet: The American Society of Hematology 2005
Fag:
Hemostasis, Thrombosis, and Vascular Biology
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC1895004/
https://ncbi.nlm.nih.gov/pubmed/15728123
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2004-05-1864
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