Nystuen, A <br/><br/>
Iraqi-Jewish kindreds with optic atrophy plus (3-methylglutaconic aciduria type 3) demonstrate linkage disequilibrium with the CTG repeat in the 3' untranslated region of the myotonic dystrophy protein kinase gene.  [electronic resource] 

 -  Human molecular genetics  Apr 1997 
 - 563-9 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0964-6906 
<br/><br/><label>Standard No.: </label>10.1093/hmg/6.4.563  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Chromosome Mapping<br/>Chromosomes, Human, Pair 19--genetics<br/>Creatine Kinase--genetics<br/>DNA Primers<br/>Female<br/>Genetic Markers<br/>Genetic Testing<br/>Genotype<br/>Glutarates--urine<br/>Humans<br/>Iraq<br/>Isoenzymes<br/>Jews<br/>Linkage Disequilibrium--genetics<br/>Lod Score<br/>Male<br/>Myotonin-Protein Kinase<br/>Optic Atrophy--genetics<br/>Pedigree<br/>Polymorphism, Genetic--genetics<br/>Protein Serine-Threonine Kinases--chemistry<br/>Trinucleotide Repeats--genetics