Yalcinkaya, Cengiz <br/><br/>
A novel GJC2 mutation associated with hypomyelination and Müllerian agenesis syndrome: coincidence or a new entity?  [electronic resource] 

 -  Neuropediatrics  Jun 2012 
 - 159-61 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1439-1899 
<br/><br/><label>Standard No.: </label>10.1055/s-0032-1313912  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Brain--pathology<br/>Connexins--genetics<br/>Demyelinating Diseases--genetics<br/>Female<br/>Humans<br/>Mullerian Ducts--abnormalities<br/>Mutation<br/>Pelizaeus-Merzbacher Disease--genetics<br/>Pelvis--abnormalities<br/>Syndrome