Bonnet-Dupeyron, Marie-Noelle <br/><br/>
Absence of OLIG2 mutations in patients presenting with a severe Pelizaeus-Merzbacher-like leukodystrophy associated with motor neuron dysfunction.  [electronic resource] 

 -  American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics  Jun 2008 
 - 538-9 p.  digital 
<br/><br/> Publication Type: Letter; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1552-485X 
<br/><br/><label>Standard No.: </label>10.1002/ajmg.b.30613  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Basic Helix-Loop-Helix Transcription Factors--genetics<br/>Demyelinating Diseases<br/>Humans<br/>Motor Neuron Disease<br/>Mutation<br/>Nerve Tissue Proteins--genetics<br/>Oligodendrocyte Transcription Factor 2<br/>Pelizaeus-Merzbacher Disease--genetics