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...

Descripción completa

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

Internet

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

Ejemplares similares