Fuchs, J <br/><br/>
Phenotypic variation in a large Swedish pedigree due to SNCA duplication and triplication.  [electronic resource] 

 -  Neurology  Mar 2007 
 - 916-22 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1526-632X 
<br/><br/><label>Standard No.: </label>10.1212/01.wnl.0000254458.17630.c5  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Aged<br/>Americas<br/>Autonomic Nervous System Diseases--genetics<br/>Blood Proteins--genetics<br/>Chromosomes, Human, Pair 4--genetics<br/>DNA Mutational Analysis<br/>Dementia--genetics<br/>Female<br/>Gene Dosage<br/>Genealogy and Heraldry<br/>Genetic Predisposition to Disease--genetics<br/>Genetic Testing<br/>Humans<br/>Male<br/>Microsatellite Repeats--genetics<br/>Middle Aged<br/>Mutation--genetics<br/>Oligonucleotide Array Sequence Analysis<br/>Parkinsonian Disorders--diagnosis<br/>Pedigree<br/>Phenotype<br/>Sweden<br/>Tomography, Emission-Computed, Single-Photon<br/>alpha-Synuclein--genetics