Pattinson, J K <br/><br/>
CRM+ haemophilia A due to a missense mutation (372----Cys) at the internal heavy chain thrombin cleavage site.  [electronic resource] 

 -  British journal of haematology  May 1990 
 - 73-7 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0007-1048 
<br/><br/><label>Standard No.: </label>10.1111/j.1365-2141.1990.tb02618.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Base Sequence<br/>DNA Mutational Analysis<br/>Dinucleoside Phosphates--genetics<br/>Factor VIII--genetics<br/>Family<br/>Female<br/>Genetic Carrier Screening<br/>Hemophilia A--genetics<br/>Humans<br/>Male<br/>Molecular Sequence Data<br/>Mutation<br/>Pedigree<br/>Polymerase Chain Reaction<br/>Polymorphism, Restriction Fragment Length<br/>Thrombin--genetics