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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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| Publicat a: | Front Genet |
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| Autors principals: | , , , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Frontiers Media S.A.
2021
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| Matèries: | |
| 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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