Mikesová, E <br/><br/>
Novel EGR2 mutation R359Q is associated with CMT type 1 and progressive scoliosis.  [electronic resource] 

 -  Neuromuscular disorders : NMD  Nov 2005 
 - 764-7 p.  digital 
<br/><br/> Publication Type: Case Reports; Comparative Study; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0960-8966 
<br/><br/><label>Standard No.: </label>10.1016/j.nmd.2005.08.001  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Arginine--genetics<br/>Charcot-Marie-Tooth Disease--complications<br/>DNA Mutational Analysis--methods<br/>DNA-Binding Proteins--genetics<br/>Female<br/>Glutamine--genetics<br/>Humans<br/>Male<br/>Mutation<br/>Neural Conduction--physiology<br/>Neurologic Examination<br/>Peripheral Nerves--physiopathology<br/>Radiography<br/>Scoliosis--complications<br/>Trans-Activators--genetics<br/>Transcriptional Regulator ERG