De la Casa-Fages, Beatriz <br/><br/>
Reply to: "Mitochondrial Parkinsonism due to SPG7/Paraplegin variants with secondary mtDNA depletion".  [electronic resource] 

 -  Movement disorders : official journal of the Movement Disorder Society  12 2019 
 - 1932-1933 p.  digital 
<br/><br/> Publication Type: Letter; Comment 
<br/><br/><label>ISSN: </label>1531-8257 
<br/><br/><label>Standard No.: </label>10.1002/mds.27899  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>ATPases Associated with Diverse Cellular Activities<br/>DNA, Mitochondrial<br/>Humans<br/>Metalloendopeptidases<br/>Paraplegia<br/>Parkinsonian Disorders<br/>Spastic Paraplegia, Hereditary