Ganji, Hamid <br/><br/>
Detection of intragenic SMN1 mutations in spinal muscular atrophy patients with a single copy of SMN1.  [electronic resource] 

 -  Journal of child neurology  Apr 2015 
 - 558-62 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1708-8283 
<br/><br/><label>Standard No.: </label>10.1177/0883073814521297  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Child, Preschool<br/>DNA Mutational Analysis<br/>Female<br/>Gene Dosage<br/>Heterozygote<br/>Humans<br/>Infant<br/>Iran<br/>Male<br/>Muscular Atrophy, Spinal--genetics<br/>Mutation<br/>Polymerase Chain Reaction<br/>Survival of Motor Neuron 1 Protein--genetics