Hereditary protein C deficiency with recurrent thrombosis: identification of a missense mutation (C6218T).

Protein C is the central component of a major anti-thrombotic regulatory system and individuals with hereditary protein C deficiency (PCD) tend to have an increased risk of thromboembolism. During the last several years, mutations causing PCD have been identified in Western countries and in Japanese...

Descripción completa

Detalles Bibliográficos
Autores principales: Song, K. S., Park, Y. S., Choi, C. R., Kim, H. K., Park, Q., Kim, H. S.
Formato: Texto
Lenguaje:English
Publicado: Korean Academy of Medical Sciences 1998
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3054489/
https://www.ncbi.nlm.nih.gov/pubmed/9610620

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3054489/
https://www.ncbi.nlm.nih.gov/pubmed/9610620

Ejemplares similares