Musa, Sara <br/><br/>
A Middle Eastern Founder Mutation Expands the Genotypic and Phenotypic Spectrum of Mitochondrial MICU1 Deficiency: A Report of 13 Patients.  [electronic resource] 

 -  JIMD reports  2019 
 - 79-83 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>2192-8304 
<br/><br/><label>Standard No.: </label>10.1007/8904_2018_107  doi