Nazli, Aisha <br/><br/>
A mutation in the TMEM65 gene results in mitochondrial myopathy with severe neurological manifestations.  [electronic resource] 

 -  European journal of human genetics : EJHG  06 2017 
 - 744-751 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1476-5438 
<br/><br/><label>Standard No.: </label>10.1038/ejhg.2017.20  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Cell Respiration<br/>Cells, Cultured<br/>Child, Preschool<br/>Female<br/>Fibroblasts--metabolism<br/>Humans<br/>Membrane Proteins--genetics<br/>Mitochondrial Encephalomyopathies--genetics<br/>Mitochondrial Membranes--metabolism<br/>Mitochondrial Proteins--genetics<br/>Mutation<br/>Oxygen--metabolism<br/>RNA Splicing