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Biochemical and cellular consequences of the antithrombin p.Met1? mutation identified in a severe thrombophilic family
Nature is always the best inspiration for basic research. A family with severe thrombosis and antithrombin deficiency, the strongest anticoagulant, carried a new mutation affecting the translation-start codon of SERPINC1, the gene encoding antithrombin. Expression of this variant in a eukaryotic cel...
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| Pubblicato in: | Oncotarget |
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| Autori principali: | , , , , , , , , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Impact Journals LLC
2018
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6145704/ https://ncbi.nlm.nih.gov/pubmed/30237862 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.18632/oncotarget.26059 |
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