Best, D Hunter <br/><br/>
Mosaic ACVRL1 and ENG mutations in hereditary haemorrhagic telangiectasia patients.  [electronic resource] 

 -  Journal of medical genetics  May 2011 
 - 358-60 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1468-6244 
<br/><br/><label>Standard No.: </label>10.1136/jmg.2010.088286  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Activin Receptors, Type II--genetics<br/>Adult<br/>Antigens, CD--genetics<br/>Base Sequence<br/>Endoglin<br/>Exons--genetics<br/>Female<br/>Humans<br/>Middle Aged<br/>Mosaicism<br/>Mutation--genetics<br/>Receptors, Cell Surface--genetics<br/>Telangiectasia, Hereditary Hemorrhagic--genetics