c.259A>C in the fibrinogen gene of alpha chain (FGA) is a fibrinogen with thrombotic phenotype

INTRODUCTION: Dysfibrinogenemia is a rare inherited disease that results from mutation in one of the three fibrinogen genes. Diagnosis can be misleading since it may present as a bleeding tendency or thrombosis and a specific coagulation test for diagnosis is not routinely available AIM: To search f...

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Detalles Bibliográficos
Autores principales: Salomon, Ophira, Barel, Ortal, Eyal, Eran, Ganor, Reut Shnerb, Kleinbaum, Yeroham, Shohat, Mordechai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2019
Materias:
Original Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6400116/
https://www.ncbi.nlm.nih.gov/pubmed/30881084
http://dx.doi.org/10.2147/TACG.S190599

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6400116/
https://www.ncbi.nlm.nih.gov/pubmed/30881084
http://dx.doi.org/10.2147/TACG.S190599

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