A large family from Argentina with Prekallikrein deficiency due to a compound heterozygosis (T insertion in intron 7 and Asp558Glu in exon 15): Prekallikrein Cordoba-Reference-Cited by-同舟云学术

A large family from Argentina with Prekallikrein deficiency due to a compound heterozygosis (T insertion in intron 7 and Asp558Glu in exon 15): Prekallikrein Cordoba

Published:2010 Issue: Volume: Page:NA-NA
ISSN:0361-8609
Container-title:American Journal of Hematology
language:en
Short-container-title:Am. J. Hematol.

Author:

Girolami Antonio,Marun Sebastian,Vettore Silvia,Scaliter Gilda,Molina Angelica,Scarparo Pamela,Tabares Aldo,Lombardi Anna Maria

Publisher

Wiley

Subject

Hematology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajh.21654/fullpdf

Reference30 articles.

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3. Thrombosis or myocardial infarction in congenital clotting factor abnormalities and chronic thrombocytopenias: A report of 21 patients and a review of 50 previously reported cases;Goodnough;Medicine (Baltimore),1983

4. Fletcher factor deficiency, source of variations of the actived partial thromboplastin time test;Entes;Am J Clin Pathol,1981

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