CFTR founder mutation causes protein trafficking defects in Chinese patients with cystic fibrosis

BACKGROUND: Cystic fibrosis (CF) is a rare condition in Asians. Since 1985, only about 30 Chinese patients have been reported with molecular confirmation. METHOD: Using our in‐house next‐generation sequencing (NGS) pipeline for childhood bronchiectasis, we identified disease‐causing CFTR mutations i...

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Detalles Bibliográficos
Autores principales: Leung, Gordon K. C., Ying, Dingge, Mak, Christopher C. Y., Chen, Xin‐Ying, Xu, Weiyi, Yeung, Kit‐San, Wong, Wai‐Lap, Chu, Yoyo W. Y., Mok, Gary T. K., Chau, Christy S. K., McLuskey, Jenna, Ong, Winnie P. T., Leong, Huey‐Yin, Chan, Kelvin Y. K., Yang, Wanling, Chen, Jeng‐Haur, Li, Albert M., Sham, Pak C., Lau, Yu‐Lung, Chung, Brian H. Y., Lee, So‐Lun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5241212/
https://www.ncbi.nlm.nih.gov/pubmed/28116329
http://dx.doi.org/10.1002/mgg3.258

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5241212/
https://www.ncbi.nlm.nih.gov/pubmed/28116329
http://dx.doi.org/10.1002/mgg3.258

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