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Targeted mutation of zebrafish fga models human congenital afibrinogenemia
Mutations in the human fibrinogen genes can lead to the absence of circulating fibrinogen and cause congenital afibrinogenemia. This rare bleeding disorder is associated with a variable phenotype, which may be influenced by environment and genotype. Here, we present a zebrafish model of afibrinogene...
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| Hoofdauteurs: | , , |
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| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
American Society of Hematology
2014
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3975262/ https://ncbi.nlm.nih.gov/pubmed/24553182 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2013-12-547182 |
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