Weiss, Karl Heinz <br/><br/>
Genetic analysis of BIRC4/XIAP as a putative modifier gene of Wilson disease.  [electronic resource] 

 -  Journal of inherited metabolic disease  Dec 2010 
 - S233-40 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1573-2665 
<br/><br/><label>Standard No.: </label>10.1007/s10545-010-9123-5  doi 
<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/>Chi-Square Distribution<br/>Child<br/>Child, Preschool<br/>Copper-Transporting ATPases<br/>DNA Mutational Analysis<br/>Female<br/>Gene Frequency<br/>Genes, Modifier<br/>Genetic Predisposition to Disease<br/>Hepatolenticular Degeneration--diagnosis<br/>Heterozygote<br/>Humans<br/>Male<br/>Middle Aged<br/>Mutation<br/>Phenotype<br/>Polymorphism, Single Nucleotide<br/>Risk Factors<br/>X-Linked Inhibitor of Apoptosis Protein--genetics<br/>Young Adult