Suzuki, S <br/><br/>
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.  [electronic resource] 

 -  Haemophilia : the official journal of the World Federation of Hemophilia  01 2018 
 - e13-e16 p.  digital 
<br/><br/> Publication Type: Letter 
<br/><br/><label>ISSN: </label>1365-2516 
<br/><br/><label>Standard No.: </label>10.1111/hae.13360  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Base Sequence<br/>Factor V Deficiency--genetics<br/>Female<br/>Hemophilia A--genetics<br/>Humans<br/>Japan<br/>Male<br/>Mannose-Binding Lectins--genetics<br/>Membrane Proteins--genetics<br/>Middle Aged<br/>Mutation<br/>Pedigree<br/>Vesicular Transport Proteins--genetics