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Systemic mast cell activation disease: the role of molecular genetic alterations in pathogenesis, heritability and diagnostics
Despite increasing understanding of its pathophysiology, the aetiology of systemic mast cell activation disease (MCAD) remains largely unknown. Research has shown that somatic mutations in kinases are necessary for the establishment of a clonal mast cell population, in particular mutations in the ty...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Blackwell Science Inc
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3482677/ https://ncbi.nlm.nih.gov/pubmed/22957768 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1365-2567.2012.03627.x |
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