Sohn, Young Bae <br/><br/>
Deletion of exons 16-17b of CFTR is frequently identified in Korean patients with cystic fibrosis.  [electronic resource] 

 -  European journal of medical genetics  Aug 2019 
 - 103681 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1878-0849 
<br/><br/><label>Standard No.: </label>10.1016/j.ejmg.2019.103681  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Alleles<br/>Child<br/>Cystic Fibrosis--genetics<br/>Cystic Fibrosis Transmembrane Conductance Regulator--genetics<br/>Exons--genetics<br/>Female<br/>Genetic Testing<br/>Humans<br/>Male<br/>Mutation--genetics<br/>Republic of Korea<br/>Sequence Deletion--genetics