Kwiatkowski, T J <br/><br/>
The gene for autosomal dominant spinocerebellar ataxia (SCA1) maps centromeric to D6S89 and shows no recombination, in nine large kindreds, with a dinucleotide repeat at the AM10 locus.  [electronic resource] 

 -  American journal of human genetics  Aug 1993 
 - 391-400 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0002-9297 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Alleles<br/>Base Sequence<br/>Centromere<br/>Child<br/>Chromosome Mapping--methods<br/>Chromosomes, Human, Pair 6<br/>Cloning, Molecular<br/>Genetic Linkage<br/>Genetic Markers<br/>Humans<br/>Lod Score<br/>Molecular Sequence Data<br/>Polymerase Chain Reaction<br/>Polymorphism, Restriction Fragment Length<br/>Recombination, Genetic<br/>Repetitive Sequences, Nucleic Acid<br/>Sequence Analysis, DNA<br/>Spinocerebellar Degenerations--genetics