Yuan, Zhe-Feng <br/><br/>
Novel mutations of the ATP7B gene in Han Chinese families with pre-symptomatic Wilson's disease.  [electronic resource] 

 -  World journal of pediatrics : WJP  Aug 2015 
 - 255-60 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1867-0687 
<br/><br/><label>Standard No.: </label>10.1007/s12519-015-0031-5  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adenosine Triphosphatases--genetics<br/>Cation Transport Proteins--genetics<br/>Child, Preschool<br/>China<br/>Cohort Studies<br/>Copper--therapeutic use<br/>Copper-Transporting ATPases<br/>Female<br/>Genetic Predisposition to Disease<br/>Genetic Testing--methods<br/>Hepatolenticular Degeneration--diagnosis<br/>Humans<br/>Infant<br/>Male<br/>Mutation<br/>Pedigree<br/>Polymorphism, Single Nucleotide<br/>Predictive Value of Tests<br/>Risk Assessment<br/>Treatment Outcome