martes, 16 de junio de 2020

Characterization of clinical and genetic spectrum of Chinese patients with cystic fibrosis | Orphanet Journal of Rare Diseases | Full Text

Characterization of clinical and genetic spectrum of Chinese patients with cystic fibrosis | Orphanet Journal of Rare Diseases | Full Text

Cystic fibrosis (CF) is a rare autosomal recessive disorder caused by biallelic mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene. The clinical features and mutation spectrum of CF ...
Authors:Keqiang Liu, Wenshuai Xu, Meng Xiao, Xinyue Zhao, Chun Bian, Qianli Zhang, Jiaxing Song, Keqi Chen, Xinlun Tian, Yaping Liu, Kai-Feng Xu and Xue Zhang
Citation:Orphanet Journal of Rare Diseases 2020 15:150
Content type:Research
 
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