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JAK2 mutations to the fore in hereditary thrombocythemia
Acquired mutations of the gene that encodes the intracellular signalling molecule JAK2 are the most frequently observed disease-driving events of the common myeloproliferative neoplasms. A number of germline JAK2 mutations have recently been described in several kindred with the rare disease of here...
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| Publicat a: | JAKSTAT |
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| Autor principal: | |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Taylor & Francis
2014
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4580080/ https://ncbi.nlm.nih.gov/pubmed/26413420 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4161/21623988.2014.957618 |
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