Hong, Young Bin <br/><br/>
A Mutation in PMP2 Causes Dominant Demyelinating Charcot-Marie-Tooth Neuropathy.  [electronic resource] 

 -  PLoS genetics  Feb 2016 
 - e1005829 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1553-7404 
<br/><br/><label>Standard No.: </label>10.1371/journal.pgen.1005829  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Sequence<br/>Animals<br/>Charcot-Marie-Tooth Disease--genetics<br/>Chromosome Segregation<br/>Computer Simulation<br/>Demyelinating Diseases--genetics<br/>Electrophysiological Phenomena<br/>Family<br/>Female<br/>Genes, Dominant<br/>HEK293 Cells<br/>Humans<br/>Leg--physiopathology<br/>Magnetic Resonance Imaging<br/>Male<br/>Mice, Transgenic<br/>Molecular Sequence Data<br/>Mutation<br/>Myelin P2 Protein--chemistry<br/>Pedigree<br/>Phenotype<br/>Sural Nerve--pathology