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Mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) in Chinese patients with congenital bilateral absence of vas deferens  Hongjun.

Published bySiri Thorstensen Modified over 5 years ago

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Presentation on theme: "Mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) in Chinese patients with congenital bilateral absence of vas deferens  Hongjun."— Presentation transcript:

1 Mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) in Chinese patients with congenital bilateral absence of vas deferens  Hongjun Li, Qiaolian Wen, Hanzhong Li, Lixi Zhao, Xinyu Zhang, Jing Wang, Longfei Cheng, Jingwen Yang, Si Chen, Xu Ma, Binbin Wang  Journal of Cystic Fibrosis  Volume 11, Issue 4, Pages (July 2012) DOI: /j.jcf Copyright © 2012 European Cystic Fibrosis Society. Terms and Conditions

2 Fig. 1 The conserved analysis in species.
Journal of Cystic Fibrosis  , DOI: ( /j.jcf ) Copyright © 2012 European Cystic Fibrosis Society. Terms and Conditions

3 Fig. 2 Schematic diagram showing putative domain-type structure of the CFTR gene. Journal of Cystic Fibrosis  , DOI: ( /j.jcf ) Copyright © 2012 European Cystic Fibrosis Society. Terms and Conditions

4 Supplement Fig. 1 Journal of Cystic Fibrosis  , DOI: ( /j.jcf ) Copyright © 2012 European Cystic Fibrosis Society. Terms and Conditions

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