Zamani, Gholam Reza <br/><br/>
Analysis of dystrophin gene in Iranian Duchenne and Becker muscular dystrophies patients and identification of a novel mutation.  [electronic resource] 

 -  Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology  Nov 2015 
 - 2011-7 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1590-3478 
<br/><br/><label>Standard No.: </label>10.1007/s10072-015-2290-2  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Child<br/>Codon, Nonsense<br/>Exons<br/>Gene Deletion<br/>Humans<br/>Iran<br/>Male<br/>Muscular Dystrophy, Duchenne--genetics<br/>Retrospective Studies<br/>Sequence Analysis, DNA--methods