Kalita, Jayantee <br/><br/>
R778L, H1069Q, and I1102T mutation study in neurologic Wilson disease.  [electronic resource] 

 -  Neurology India   
 - 627-30 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0028-3886 
<br/><br/><label>Standard No.: </label>10.4103/0028-3886.68678  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adenosine Triphosphatases--genetics<br/>Adolescent<br/>Adult<br/>Amino Acids--genetics<br/>Cation Transport Proteins--genetics<br/>Child<br/>Child, Preschool<br/>Copper-Transporting ATPases<br/>DNA Mutational Analysis--methods<br/>Family Health<br/>Female<br/>Gene Frequency<br/>Hepatolenticular Degeneration--genetics<br/>Humans<br/>India<br/>Magnetic Resonance Imaging--methods<br/>Male<br/>Mutation--genetics<br/>Severity of Illness Index<br/>Young Adult