Yu, C E <br/><br/>
Mutations in the consensus helicase domains of the Werner syndrome gene. Werner's Syndrome Collaborative Group.  [electronic resource] 

 -  American journal of human genetics  Feb 1997 
 - 330-41 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0002-9297 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Asian People--genetics<br/>Consensus Sequence<br/>DNA Helicases--chemistry<br/>Exodeoxyribonucleases<br/>Exons<br/>Frameshift Mutation<br/>Haplotypes<br/>Heterozygote<br/>Humans<br/>Introns<br/>Japan<br/>Molecular Sequence Data<br/>Mutation<br/>Phenotype<br/>Point Mutation<br/>RecQ Helicases<br/>Sequence Deletion<br/>Werner Syndrome--genetics<br/>Werner Syndrome Helicase<br/>White People--genetics