Fabrizi, G M <br/><br/>
PMP22 related congenital hypomyelination neuropathy.  [electronic resource] 

 -  Journal of neurology, neurosurgery, and psychiatry  Jan 2001 
 - 123-6 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0022-3050 
<br/><br/><label>Standard No.: </label>10.1136/jnnp.70.1.123  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Demyelinating Diseases--genetics<br/>Female<br/>Humans<br/>Myelin Proteins--genetics<br/>Point Mutation--genetics<br/>Sural Nerve--pathology