Muglia, Maria <br/><br/>
A novel founder mutation in the MFN2 gene associated with variable Charcot-Marie-Tooth type 2 phenotype in two families from Southern Italy.  [electronic resource] 

 -  BMJ case reports  2009 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1757-790X 
<br/><br/><label>Standard No.: </label>10.1136/bcr.08.2008.0652  doi