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pro vyhledávání: '"Binmethem, Alanoud"'
Autor:
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
Publikováno v:
Nagoya Journal of Medical Science. 83(3):407-417
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 Ad
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=jairo_______::3a3db8580a3ec55a915a4d6c7f871876
https://nagoya.repo.nii.ac.jp/records/2001435
https://nagoya.repo.nii.ac.jp/records/2001435
