The prevalence of Factor V Leiden (Arg506Gln) mutation in King Khalid University Hospital patients, 2017–2019

Arg506Gln mutation is responsible for one of the procoagulant factors and most common inherited thrombophilia in the Factor V Leiden (FVL) family. The replacement of the missense mutation for Arg506Gln / R506Q is at 1691st position from Guanine to Adenine with the modification of the amino acid from...

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Detalles Bibliográficos
Autores principales: Al-Otaiby, Maram, Althnayan, Rahaf, Binmethem, Alanoud, AlEnezy, Reema Bader, Alhadlg, Munira Abdulrahman, Alaqeel, Arjuwana, AlQahtani, Sara H, Ghufran, Noman, Alotaibi, Abdulaziz A., Alayed, Nada, Ali Khan, Imran
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nagoya University 2021
Materias:
Original Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8438009/
https://www.ncbi.nlm.nih.gov/pubmed/34552279
http://dx.doi.org/10.18999/nagjms.83.3.407

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