Bartsch, J W <br/><br/>
The protein kinase N (PKN) gene PRKCL1/Prkcl1 maps to human chromosome 19p12-p13.1 and mouse chromosome 8 with close linkage to the myodystrophy (myd) mutation.  [electronic resource] 

 -  Genomics  Apr 1998 
 - 129-32 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0888-7543 
<br/><br/><label>Standard No.: </label>10.1006/geno.1997.5208  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Animals<br/>Chromosome Mapping<br/>Chromosomes, Human, Pair 19<br/>Female<br/>Genetic Linkage<br/>Humans<br/>In Situ Hybridization, Fluorescence<br/>Male<br/>Mice<br/>Mice, Inbred C57BL<br/>Muscular Dystrophy, Animal--genetics<br/>Mutation<br/>Protein Kinase C--genetics