Mainz, J <br/><br/>
Cystic fibrosis in 65- and 67-year-old siblings. Clinical feature and nasal potential difference measurement in patients with genotypes F508del and 2789+5G-->A.  [electronic resource] 

 -  Respiration; international review of thoracic diseases  2006 
 - 698-704 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>0025-7931 
<br/><br/><label>Standard No.: </label>10.1159/000093818  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Aged<br/>Amiloride<br/>Chlorides--analysis<br/>Cystic Fibrosis--diagnosis<br/>Cystic Fibrosis Transmembrane Conductance Regulator--genetics<br/>Genetic Carrier Screening<br/>Genotype<br/>Humans<br/>Male<br/>Membrane Potentials<br/>Nasal Mucosa--physiology<br/>Phenotype<br/>Siblings<br/>Sweat--chemistry