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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Detalles Bibliográficos
Publicado en:Oncotarget
Main Authors: Navarro-Fernández, José, Eugenia de la Morena-Barrio, María, Martínez-Alonso, Emma, Dybedal, Ingunn, Toderici, Mara, Bohdan, Nataliya, Miñano, Antonia, Heimdal, Ketil, Abildgaard, Ulrich, Martínez-Menárguez, José Ángel, Corral, Javier, Vicente, Vicente
Formato: Artigo
Idioma:Inglês
Publicado: Impact Journals LLC 2018
Assuntos:
Research Paper
Acceso en liña: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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