Akagawa, Hiroyuki <br/><br/>
A case of delayed-onset hereditary hemorrhagic telangiectasia with a frameshift ENG mutation.  [electronic resource] 

 -  Neurology India   
 - 312-314 p.  digital 
<br/><br/> Publication Type: Case Reports; Letter 
<br/><br/><label>ISSN: </label>0028-3886 
<br/><br/><label>Standard No.: </label>10.4103/0028-3886.253633  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Activin Receptors, Type II--genetics<br/>Aged<br/>Endoglin--genetics<br/>Female<br/>Humans<br/>Mutation--genetics<br/>Telangiectasia, Hereditary Hemorrhagic--diagnosis