Identification of a Mutation in the Novel Compound Heterozygous CFTR in a Chinese Family with Cystic Fibrosis

Cystic fibrosis (CF) is one of the most common autosomal recessive disorders among Caucasians of Northern European descent but is uncommon in the Chinese population. Objectives. To elucidate the mutation in the novel compound heterozygous CFTR causing CF in Chinese family. Materials and Methods. Cli...

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Bibliographic Details
Published in:Can Respir J
Main Authors: Shao, Hongxia, Hua, Jingna, Wu, Qi, Li, Xiaoge, Zhang, Ming, Wang, Herong, Wu, Junping, Xu, Long, Xie, Yi, Li, Li, Chen, Huaiyong
Format: Artigo
Language:Inglês
Published: Hindawi 2020
Subjects:
Clinical Study
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC7229557/
https://ncbi.nlm.nih.gov/pubmed/32454915
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2020/6507583
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