Open AccessA case Report of a Classic Cystic fibrosis Pediatric Patient in Korea Carrying Very Rare CFTR Gene Mutations (D993Y and Q220X)
Author(s) -
Min Jung Kim,
Jung Wan Kang,
Ji Hyun Lee,
Kyung Won Kim,
Myung Hyun Sohn,
Min Goo Lee,
MyungJoon Kim,
Kyu-Earn Kim
Publication year - 2011
Publication title -
pediatric allergy and respiratory disease
Language(s) - English
Resource type - Journals
ISSN - 1225-679X
DOI - 10.7581/pard.2011.21.1.61
Subject(s) - cystic fibrosis , medicine , cystic fibrosis transmembrane conductance regulator , failure to thrive , disease , chloride channel , mutation , gene , infertility , pathology , genetics , biology , pregnancy , microbiology and biotechnology
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