Bannwarth, Sylvie <br/><br/>
Reply: A distinct clinical phenotype in a German kindred with motor neuron disease carrying a CHCHD10 mutation.  [electronic resource] 

 -  Brain : a journal of neurology  Sep 2015 
 - e377 p.  digital 
<br/><br/> Publication Type: Letter; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Comment 
<br/><br/><label>ISSN: </label>1460-2156 
<br/><br/><label>Standard No.: </label>10.1093/brain/awv015  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amyotrophic Lateral Sclerosis--etiology<br/>DNA, Mitochondrial--genetics<br/>Female<br/>Frontotemporal Dementia--etiology<br/>Humans<br/>Male<br/>Mitochondria--pathology<br/>Mitochondrial Diseases--complications<br/>Mitochondrial Proteins--genetics