Aminkeng, F <br/><br/>
PDGFRB mutation causes autosomal-dominant Penttinen syndrome.  [electronic resource] 

 -  Clinical genetics  Dec 2015 
 - 531 p.  digital 
<br/><br/> Publication Type: Journal Article; Comment 
<br/><br/><label>ISSN: </label>1399-0004 
<br/><br/><label>Standard No.: </label>10.1111/cge.12680  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Acro-Osteolysis--genetics<br/>Female<br/>Humans<br/>Limb Deformities, Congenital--genetics<br/>Male<br/>Point Mutation--genetics<br/>Progeria--genetics<br/>Receptor, Platelet-Derived Growth Factor beta--genetics<br/>Signal Transduction--genetics