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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Dades bibliogràfiques
Publicat a:Front Genet
Autors principals: Yang, Dongshan, Liang, Xiubin, Pallas, Brooke, Hoenerhoff, Mark, Ren, Zhuoying, Han, Renzhi, Zhang, Jifeng, Chen, Y. Eugene, Jin, Jian-Ping, Sun, Fei, Xu, Jie
Format: Artigo
Idioma:Inglês
Publicat: Frontiers Media S.A. 2021
Matèries:
Genetics
Accés en línia: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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