Zhang, Chao <br/><br/>
Ataxia with novel compound heterozygous PEX10 mutations and a literature review of PEX10-related peroxisome biogenesis disorders.  [electronic resource] 

 -  Clinical neurology and neurosurgery  02 2019 
 - 92-96 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Review 
<br/><br/><label>ISSN: </label>1872-6968 
<br/><br/><label>Standard No.: </label>10.1016/j.clineuro.2019.01.004  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Cerebellar Ataxia--diagnosis<br/>Child<br/>Genetic Testing--methods<br/>Humans<br/>Male<br/>Mutation--genetics<br/>Peroxins--genetics<br/>Peroxisomal Disorders--diagnosis<br/>Receptors, Cytoplasmic and Nuclear--genetics