Nazé, Peggy <br/><br/>
Mutation analysis and association studies of the ubiquitin carboxy-terminal hydrolase L1 gene in Huntington's disease.  [electronic resource] 

 -  Neuroscience letters  Aug 2002 
 - 1-4 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0304-3940 
<br/><br/><label>Standard No.: </label>10.1016/s0304-3940(02)00231-8  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Age of Onset<br/>Aging--genetics<br/>Base Sequence--genetics<br/>Cysteine Endopeptidases--genetics<br/>DNA Mutational Analysis<br/>Female<br/>Gene Frequency--genetics<br/>Genetic Testing<br/>Genetic Variation--genetics<br/>Genotype<br/>Humans<br/>Huntington Disease--enzymology<br/>Linkage Disequilibrium--genetics<br/>Male<br/>Middle Aged<br/>Molecular Sequence Data<br/>Multienzyme Complexes--genetics<br/>Mutation--genetics<br/>Polymorphism, Genetic--genetics<br/>Proteasome Endopeptidase Complex<br/>Thiolester Hydrolases--deficiency<br/>Trinucleotide Repeat Expansion--genetics<br/>Ubiquitin Thiolesterase