Gollob, M H <br/><br/>
Identification of a gene responsible for familial Wolff-Parkinson-White syndrome.  [electronic resource] 

 -  The New England journal of medicine  Jun 2001 
 - 1823-31 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0028-4793 
<br/><br/><label>Standard No.: </label>10.1056/NEJM200106143442403  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>AMP-Activated Protein Kinases<br/>Base Sequence<br/>Chromosome Mapping<br/>Chromosomes, Human, Pair 7<br/>Female<br/>Genes, Dominant<br/>Haplotypes<br/>Humans<br/>Lod Score<br/>Male<br/>Multienzyme Complexes--genetics<br/>Mutation, Missense<br/>Pedigree<br/>Protein Serine-Threonine Kinases--genetics<br/>Wolff-Parkinson-White Syndrome--genetics