van de Wetering, R A C <br/><br/>
Hereditary neuropathy with liability to pressure palsies with a small deletion interrupting the PMP22 gene.  [electronic resource] 

 -  Neuromuscular disorders : NMD  Oct 2002 
 - 651-5 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>0960-8966 
<br/><br/><label>Standard No.: </label>10.1016/s0960-8966(02)00025-1  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Blotting, Southern<br/>Hereditary Sensory and Motor Neuropathy--genetics<br/>Humans<br/>Male<br/>Myelin Proteins--genetics<br/>Paralysis--genetics<br/>Pressure