Deletion of exons 16–17b of CFTR is frequently identified in Korean patients with cystic fibrosis-Reference-Cited by-同舟云学术

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Deletion of exons 16–17b of CFTR is frequently identified in Korean patients with cystic fibrosis

Published:2019-08 Issue:8 Volume:62 Page:103681
ISSN:1769-7212
Container-title:European Journal of Medical Genetics
language:en
Short-container-title:European Journal of Medical Genetics

Author:

Sohn Young Bae,Ko Jung Min,Jang Ju Young,Seong Moon-Woo,Park Sung Sup,Suh Dong In,Ko Jae Sung,Shin Choong-Ho

Funder

National Research Foundation of Korea

Ministry of Science, ICT & Future Planning

Publisher

Elsevier BV

Subject

Genetics(clinical),Genetics,General Medicine

Reference29 articles.

1. Cystic fibrosis in Korean children:a case report identified by a quantitative pilocarpine iontophoresis sweat test and genetic analysis;Ahn;J. Korean Med. Sci.,2005

2. Ethnicity impacts the cystic fibrosis diagnosis: a note of caution;Bosch;J. Cyst. Fibros. : Off. J. Europe. Cystic. Fibros. Soc.,2017

3. A new era in the treatment of cystic fibrosis: correction of the underlying CFTR defect;Boyle;Lancet. Resp. .Med.,2013

4. Cystic fibrosis: a review of associated phenotypes, use of molecular diagnostic approaches, genetic characteristics, progress, and dilemmas;Brennan;J. Mol. Diagn. : J. Mod. Dyn.,2016

5. Novel CFTR mutations in a Korean infant with cystic fibrosis and pancreatic insufficiency;Choe;J. Korean Med. Sci.,2010

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