Waters, M F <br/><br/>
An autosomal dominant ataxia maps to 19q13: Allelic heterogeneity of SCA13 or novel locus?  [electronic resource] 

 -  Neurology  Oct 2005 
 - 1111-3 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>1526-632X 
<br/><br/><label>Standard No.: </label>10.1212/01.wnl.0000177490.05162.41  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Aged<br/>Aged, 80 and over<br/>Chromosome Disorders--genetics<br/>Chromosome Mapping<br/>Chromosomes, Human, Pair 19--genetics<br/>DNA Mutational Analysis<br/>Female<br/>Genes, Dominant--genetics<br/>Genetic Linkage--genetics<br/>Genetic Predisposition to Disease--genetics<br/>Genetic Testing<br/>Genotype<br/>Haplotypes<br/>Humans<br/>Male<br/>Middle Aged<br/>Mutation--genetics<br/>Pedigree<br/>Penetrance<br/>Phenotype<br/>Philippines<br/>Spinocerebellar Ataxias--genetics