Clain, Jérôme <br/><br/>
A neutral variant involved in a complex CFTR allele contributes to a severe cystic fibrosis phenotype.  [electronic resource] 

 -  Human genetics  May 2005 
 - 454-60 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0340-6717 
<br/><br/><label>Standard No.: </label>10.1007/s00439-004-1246-z  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alleles<br/>Chloride Channels--metabolism<br/>Cystic Fibrosis--genetics<br/>Cystic Fibrosis Transmembrane Conductance Regulator--genetics<br/>Genes, Recessive<br/>Genetic Variation<br/>HeLa Cells<br/>Humans<br/>Mutation<br/>Phenotype<br/>Polymorphism, Genetic