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Identification of MPL R102P Mutation in Hereditary Thrombocytosis
The molecular basis of hereditary thrombocytosis is germline mutations affecting the thrombopoietin (TPO)/TPO receptor (MPL)/JAK2 signaling axis. Here, we report one family presenting two cases with a mild thrombocytosis. By sequencing JAK2 and MPL coding exons, we identified a germline MPL R102P he...
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| Publicat a: | Front Endocrinol (Lausanne) |
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| Autors principals: | , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Frontiers Media S.A.
2017
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5611484/ https://ncbi.nlm.nih.gov/pubmed/28979237 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fendo.2017.00235 |
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