Patel, A J <br/><br/>
Successful percutaneous coronary intervention in a patient with combined deficiency of FV and FVIII due to novel compound heterozygous mutations in LMAN1.  [electronic resource] 

 -  Haemophilia : the official journal of the World Federation of Hemophilia  Jul 2013 
 - 607-10 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, N.I.H., Extramural 
<br/><br/><label>ISSN: </label>1365-2516 
<br/><br/><label>Standard No.: </label>10.1111/hae.12128  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Aged<br/>Coronary Angiography<br/>Factor V--metabolism<br/>Factor V Deficiency--complications<br/>Factor VIII--metabolism<br/>Hemophilia A--complications<br/>Heterozygote<br/>Humans<br/>Male<br/>Mannose-Binding Lectins--genetics<br/>Membrane Proteins--genetics<br/>Mutation--genetics<br/>Percutaneous Coronary Intervention