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Conclusions In summary, a comprehensive characterization and analysis of the NtGST s at the genome level were performed in this study

Abstract Cystic Fibrosis (CF), a multi-organ disease stemming from CFTR gene mutations, is characterized by progressive pulmonary disease, chronic inflammation, and a pro-oxidative environment
[DOI] [PMC free article] [PubMed] [Google Scholar] 115.Liu F., Zhu Y., Zhang J., Li Y., Peng Z

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