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Detection of single nucleotide polymorphisms in coagulation factor XI deficient patients by multitemperature single‐strand conformation polymorphism analysis
Factor XI (FXI) deficiency is a rare inherited disorder which can cause bleeding complications especially in case of hemostatic challenge and/or in tissues with high fibrinolytic activity. A number of causative mutations have been described in FXI deficient individuals which have been detected by va...
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| Publicado no: | J Clin Lab Anal |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Wiley Subscription Services, Inc., A Wiley Company
2005
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6807907/ https://ncbi.nlm.nih.gov/pubmed/16302212 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jcla.20084 |
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