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Publikováno v:
Infection and Drug Resistance
Cystic Fibrosis (CF) is an autosomal recessive disease characterized by a mutation in the cystic fibrosis transmembrane conductance regulator (CFTR) protein. Impairment of the CFTR protein in the respiratory tract results in the formation of thick mu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55126ac1b804378282afdc7edd8a198a
https://pubmed.ncbi.nlm.nih.gov/33790585
https://pubmed.ncbi.nlm.nih.gov/33790585
