Santhosh, S <br/><br/>
ATP7B mutations in families in a predominantly Southern Indian cohort of Wilson's disease patients.  [electronic resource] 

 -  Indian journal of gastroenterology : official journal of the Indian Society of Gastroenterology   
 - 277-82 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0254-8860 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adenosine Triphosphatases--genetics<br/>Adolescent<br/>Adult<br/>Age of Onset<br/>Cation Transport Proteins--genetics<br/>Ceruloplasmin--analysis<br/>Child<br/>Codon<br/>Consanguinity<br/>Copper--urine<br/>Copper-Transporting ATPases<br/>Exons<br/>Female<br/>Hepatolenticular Degeneration--genetics<br/>Humans<br/>India<br/>Male<br/>Middle Aged<br/>Mutation<br/>Phenotype<br/>Polymorphism, Genetic