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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)...

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Detalles Bibliográficos
Autores principales: Zheng, Baoying, Cao, Ling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
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.
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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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