Extensive genetic screening of Iranian Factor FVII-deficient individuals unraveled several novel mutations and postulated founder effects in some cases-Reference-Cited by-同舟云学术

Extensive genetic screening of Iranian Factor FVII-deficient individuals unraveled several novel mutations and postulated founder effects in some cases

Published:2023-01 Issue:1 Volume:7 Page:100003
ISSN:2475-0379
Container-title:Research and Practice in Thrombosis and Haemostasis
language:en
Short-container-title:Research and Practice in Thrombosis and Haemostasis

Author:

Ravanbod Shirin,Faranoush Mohammad,Changi-Ashtiani Majid,Rokni-Zadeh Hassan,Shahani Tina

Publisher

Elsevier BV

Subject

Hematology

Reference36 articles.

1. Inherited factor VII deficiency: molecular genetics and pathophysiology;Cooper;Thromb Haemost,1997

2. Factor VII deficiency and the FVII mutation database;McVey;Hum Mutat,2001

3. A model for the tissue factor pathway to thrombin. I. An empirical study;Lawson;J Biol Chem,1994

4. Molecular analysis of the genotype-phenotype relationship in factor VII deficiency;Millar;Hum Genet,2000

5. Clinical manifestations in 28 Italian and Iranian patients with severe factor VII deficiency;Peyvandi;Haemophilia,1997

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