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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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Detalles Bibliográficos
Autores principales:	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:	Online Artículo Texto
Lenguaje:	English
Publicado:	Impact Journals LLC 2018
Materias:	Research Paper
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6145704/ https://www.ncbi.nlm.nih.gov/pubmed/30237862 http://dx.doi.org/10.18632/oncotarget.26059

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