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                                       Details for article 1 of 32 found articles
 
 
  A case of congenital prothrombin deficiency with two concurrent mutations in the prothrombin gene
 
 
Title: A case of congenital prothrombin deficiency with two concurrent mutations in the prothrombin gene
Author: Mansory, Eman M.
Bhai, Pratibha
Stuart, Alan
Laudenbach, Lori
Sadikovic, Bekim
Lazo‐Langner, Alejandro
Appeared in: Research and practice in thrombosis and haemostasis
Paging: Volume 5 () nr. 4 pages p.
Year: 2021
Contents:
Publisher: The Authors. Research and Practice in Thrombosis and Haemostasis published by Wiley Periodicals LLC on behalf of International Society on Thrombosis and Haemostasis (ISTH)
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

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