A deep vein thrombosis caused by 20209C>T mutation in homozygosis of the prothrombin gene in a Caucasian patient

INTRODUCTION: Additional nucleotide substitutions in the 3′-untranslated region of prothrombin gene could explain some thrombotic events and also adverse pregnancy outcomes. We describe the first case of a homozygous 20209C>T mutation as the cause of deep vein thrombosis in a Spanish patient. CAS...

Descripción completa

Detalles Bibliográficos
Autores principales: Álvarez, Silvia Izquierdo, Ollero, Eva Barrio, Llinares Sanjuan, Francisco Miguel, Martínez, Fabiola Lorente, Calvo Martín, María Teresa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Croatian Society of Medical Biochemistry and Laboratory Medicine 2014
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3936973/
https://www.ncbi.nlm.nih.gov/pubmed/24627725
http://dx.doi.org/10.11613/BM.2014.018

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3936973/
https://www.ncbi.nlm.nih.gov/pubmed/24627725
http://dx.doi.org/10.11613/BM.2014.018

Ejemplares similares