Nanetti, Lorenzo <br/><br/>
ANO10 mutational screening in recessive ataxia: genetic findings and refinement of the clinical phenotype.  [electronic resource] 

 -  Journal of neurology  Feb 2019 
 - 378-385 p.  digital 
<br/><br/> Publication Type: Journal Article; Observational Study 
<br/><br/><label>ISSN: </label>1432-1459 
<br/><br/><label>Standard No.: </label>10.1007/s00415-018-9141-z  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Anoctamins--genetics<br/>Cognitive Dysfunction--physiopathology<br/>Disease Progression<br/>Evoked Potentials, Somatosensory--physiology<br/>Executive Function--physiology<br/>Female<br/>Genes, Recessive<br/>Humans<br/>Male<br/>Middle Aged<br/>Mutation<br/>Pedigree<br/>Spinocerebellar Ataxias--genetics