Chelban, Viorica <br/><br/>
Genotype-phenotype correlations, dystonia and disease progression in spinocerebellar ataxia type 14.  [electronic resource] 

 -  Movement disorders : official journal of the Movement Disorder Society  07 2018 
 - 1119-1129 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1531-8257 
<br/><br/><label>Standard No.: </label>10.1002/mds.27334  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Age of Onset<br/>Aged<br/>Child, Preschool<br/>Cohort Studies<br/>Cysteine--genetics<br/>Disease Progression<br/>Dystonia--etiology<br/>Family Health<br/>Female<br/>Genetic Association Studies<br/>Genetic Testing<br/>Humans<br/>Magnetic Resonance Imaging<br/>Male<br/>Middle Aged<br/>Mutation, Missense--genetics<br/>Peptides--genetics<br/>Phenotype<br/>Protein Kinase C--genetics<br/>Spinocerebellar Ataxias--complications<br/>Young Adult