HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Prothrombin 20210A mutation in acute posterior cerebral artery infarction and branch retinal vein occlusion.

AuthorsSruti S Rachapudi, Chaow Charoenkijkajorn, Mohammad Pakravan, Andrew G Lee
JournalCanadian journal of ophthalmology. Journal canadien d'ophtalmologie (Can J Ophthalmol) Vol. 58 Issue 6 Pg. e259-e262 (12 2023) ISSN: 1715-3360 [Electronic] England
PMID37545047 (Publication Type: Letter)
Chemical References
  • Prothrombin
Topics
  • Humans
  • Retinal Vein Occlusion (diagnosis, genetics)
  • Prothrombin (genetics)
  • Infarction, Posterior Cerebral Artery
  • Genotype
  • Mutation
  • Retinal Artery Occlusion

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: