Combined deficiency of factors V and VIII by chance coinheritance of parahaemophilia and haemophilia A, but not by mutations of either LMAN1 or MCFD2, in a Japanese family

Publisher： John Wiley & Sons Inc

E-ISSN： 1365-2516|24|1|e13-e16

ISSN： 1351-8216

Source： HAEMOPHILIA, Vol.24, Iss.1, 2018-01, pp. : e13-e16

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Related content

Successful abdominal operation without replacement therapy in a patient with combined factor V (FV) and FVIII deficiency due to novel homozygous mutation in LMAN1

By  

HAEMOPHILIA, Vol. 21, Iss. 6, 2015-11 ,pp. : e492-e494

John Wiley & Sons Inc

Access to resources Recommend Favorite

A synonymous mutation in LMAN1 creates an ectopic splice donor site and causes combined deficiency of FV and FVIII

By  

JOURNAL OF THROMBOSIS AND HAEMOSTASIS, Vol. 10, Iss. 11, 2012-11 ,pp. : 2407-2409

John Wiley & Sons Inc

Access to resources Recommend Favorite

Successful Use of Factor VIII Concentrate and Fresh Frozen Plasma for Four Dental Extractions in an Individual with Combined Factor V and VIII Deficiency

By  

Transfusion Medicine and Hemotherapy, Vol. 36, Iss. 2, 2009-03 ,pp. : 138-139

Karger

Access to resources Recommend Favorite

Usefulness of an in vitro cellular expression model for haemophilia A carrier diagnosis: illustration with five novel mutations in the F8 gene in women with isolated factor VIII:C deficiency

By  

HAEMOPHILIA, Vol. 21, Iss. 3, 2015-05 ,pp. : e202-e209

John Wiley & Sons Inc

Access to resources Recommend Favorite

Factor VIII Inhibitors in Two Families with Mild Haemophilia A: Structural Analysis of the Mutations

By  

Pathophysiology of Haemostasis and Thrombosis, Vol. 30, Iss. 5, 2001-03 ,pp. : 268-279

Karger

Access to resources Recommend Favorite