Muglia, Maria <br/><br/>
A novel point mutation in PMP22 gene in an Italian family with hereditary neuropathy with liability to pressure palsies.  [electronic resource] 

 -  Journal of the neurological sciences  Dec 2007 
 - 194-7 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0022-510X 
<br/><br/><label>Standard No.: </label>10.1016/j.jns.2007.05.034  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Chromosomes, Human, Pair 17<br/>DNA Mutational Analysis--methods<br/>Exons--genetics<br/>Family Health<br/>Female<br/>Hereditary Sensory and Motor Neuropathy--complications<br/>Humans<br/>Italy<br/>Male<br/>Middle Aged<br/>Myelin Proteins--genetics<br/>Neural Conduction--physiology<br/>Paralysis--complications<br/>Point Mutation<br/>Pressure