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Differences in gene mutations between Chinese and Caucasian cystic fibrosis patients
Cystic fibrosis (CF) is rarely seen in Asian populations. We diagnosed two CF cases. One of them had a novel mutation c.870‐1G>C in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. There have been 38 Chinese CF patients reported in literature from 1974 until the present (2016)...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5324682/ https://www.ncbi.nlm.nih.gov/pubmed/27717243 http://dx.doi.org/10.1002/ppul.23539 |
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author | Zheng, Baoying Cao, Ling |
author_facet | Zheng, Baoying Cao, Ling |
author_sort | Zheng, Baoying |
collection | PubMed |
description | Cystic fibrosis (CF) is rarely seen in Asian populations. We diagnosed two CF cases. One of them had a novel mutation c.870‐1G>C in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. There have been 38 Chinese CF patients reported in literature from 1974 until the present (2016), 25 different mutations were identified. Only one of these mutations (R553X) is in the Caucasian CF screening panel. The mutations identified in Chinese CF patients are very different from the common Caucasian gene mutations. The CFTR gene mutation spectrum for the Chinese population requires further investigation. Pediatr Pulmonol. 2017;52:E11–E14. © 2016 The Authors. Pediatric Pulmonology Published by Wiley Periodicals, Inc. |
format | Online Article Text |
id | pubmed-5324682 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-53246822017-03-14 Differences in gene mutations between Chinese and Caucasian cystic fibrosis patients Zheng, Baoying Cao, Ling Pediatr Pulmonol Case Report Published Online Cystic fibrosis (CF) is rarely seen in Asian populations. We diagnosed two CF cases. One of them had a novel mutation c.870‐1G>C in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. There have been 38 Chinese CF patients reported in literature from 1974 until the present (2016), 25 different mutations were identified. Only one of these mutations (R553X) is in the Caucasian CF screening panel. The mutations identified in Chinese CF patients are very different from the common Caucasian gene mutations. The CFTR gene mutation spectrum for the Chinese population requires further investigation. Pediatr Pulmonol. 2017;52:E11–E14. © 2016 The Authors. Pediatric Pulmonology Published by Wiley Periodicals, Inc. John Wiley and Sons Inc. 2016-10-07 2017-03 /pmc/articles/PMC5324682/ /pubmed/27717243 http://dx.doi.org/10.1002/ppul.23539 Text en © 2016 The Authors. Pediatric Pulmonology Published by Wiley Periodicals, Inc. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Case Report Published Online Zheng, Baoying Cao, Ling Differences in gene mutations between Chinese and Caucasian cystic fibrosis patients |
title | Differences in gene mutations between Chinese and Caucasian cystic fibrosis patients |
title_full | Differences in gene mutations between Chinese and Caucasian cystic fibrosis patients |
title_fullStr | Differences in gene mutations between Chinese and Caucasian cystic fibrosis patients |
title_full_unstemmed | Differences in gene mutations between Chinese and Caucasian cystic fibrosis patients |
title_short | Differences in gene mutations between Chinese and Caucasian cystic fibrosis patients |
title_sort | differences in gene mutations between chinese and caucasian cystic fibrosis patients |
topic | Case Report Published Online |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5324682/ https://www.ncbi.nlm.nih.gov/pubmed/27717243 http://dx.doi.org/10.1002/ppul.23539 |
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