Highsmith, W E <br/><br/>
A CFTR mutation (D1152H) in a family with mild lung disease and normal sweat chlorides.  [electronic resource] 

 -  Clinical genetics  Jul 2005 
 - 88-90 p.  digital 
<br/><br/> Publication Type: Letter; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0009-9163 
<br/><br/><label>Standard No.: </label>10.1111/j.1399-0004.2005.00459.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Aged<br/>Chlorides<br/>Cystic Fibrosis--etiology<br/>Cystic Fibrosis Transmembrane Conductance Regulator--genetics<br/>Family<br/>Female<br/>Humans<br/>Lung Diseases--etiology<br/>Male<br/>Middle Aged<br/>Mutation<br/>Reference Values<br/>Sweat