Congenital factor XIII deficiency in Pakistan: characterization of seven families and identification of four novel mutations-Reference-Cited by-同舟云学术

Congenital factor XIII deficiency in Pakistan: characterization of seven families and identification of four novel mutations

Published:2013-12-16 Issue:4 Volume:20 Page:568-574
ISSN:1351-8216
Container-title:Haemophilia
language:en
Short-container-title:Haemophilia

Author:

Borhany M.¹,Handrkova H.²,Cairo A.³,Schroeder V.²,Fatima N.¹,Naz A.¹,Amanat S.⁴,Shamsi T.¹,Peyvandi F.³,Kohler H. P.²⁵

Affiliation:

1. Department of Haematology, Haemostasis & Thrombosis; National Institute of Blood Disease and Bone Marrow Transplantation (NIBD); Karachi Pakistan

2. Haemostasis Research Laboratory; University Clinic of Haematology; University Hospital & University of Bern; Bern Switzerland

3. U.O.S. Dipartimentale per la Diagnosi e la Terapia delle Coagulopatie; A. Bianchi Bonomi Hemophilia and Thrombosis Center; Fondazione I.R.C.C.S. Cà Granda Ospedale Maggiore Policlinico; Università degli Studi di Milano and Luigi Villa Foundation; Milan Italy

4. PAEC Hospital; Islamabad Pakistan

5. Department of Internal Medicine; Spital Netz Bern; Bern Switzerland

Publisher

Wiley

Subject

Genetics(clinical),Hematology,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/hae.12340/fullpdf

Reference27 articles.

1. Coagulation factor activity and clinical bleeding severity in rare bleeding disorders: results from the European Network of Rare Bleeding Disorders;Peyvandi;J Thromb Haemost,2012

2. Factor XIII: a coagulation factor with multiple plasmatic and cellular functions;Muszbek;Physiol Rev,2011

3. Factor XIII deficiency;Karimi;Semin Thromb Hemost,2009