Production of CFTR-ΔF508 Rabbits

Cystic Fibrosis (CF) is a lethal autosomal recessive disease caused by mutations in the gene encoding the cystic fibrosis transmembrane conductance regulator (CFTR). The most common mutation is the deletion of phenylalanine residue at position 508 (ΔF508). Here we report the production of CFTR-ΔF508...

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Detalhes bibliográficos
Publicado no:Front Genet
Main Authors: Yang, Dongshan, Liang, Xiubin, Pallas, Brooke, Hoenerhoff, Mark, Ren, Zhuoying, Han, Renzhi, Zhang, Jifeng, Chen, Y. Eugene, Jin, Jian-Ping, Sun, Fei, Xu, Jie
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2021
Assuntos:
Genetics
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7862758/
https://ncbi.nlm.nih.gov/pubmed/33552140
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2020.627666
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