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The Nbeal2(−/−) mouse as a model for the gray platelet syndrome
The gray platelet syndrome (GPS) is a rare, autosomal-recessive platelet disorder characterized by thrombocytopenia, large platelets lacking α-granules, and variable bleeding. GPS has been linked to mutations in the neurobeachin-like 2 gene (NBEAL2). We have recently characterized Nbeal2-deficient m...
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| Päätekijät: | , , , , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
Landes Bioscience
2013
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3915564/ https://ncbi.nlm.nih.gov/pubmed/25003009 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4161/rdis.26561 |
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