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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7862758/
https://www.ncbi.nlm.nih.gov/pubmed/33552140
http://dx.doi.org/10.3389/fgene.2020.627666

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7862758/
https://www.ncbi.nlm.nih.gov/pubmed/33552140
http://dx.doi.org/10.3389/fgene.2020.627666

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