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Abstract Cystic fibrosis is an autosomal recessive, monogenetic disorder caused by mutations in the cystic fibrosis transmembrane conductance regulator ( CFTR ) gene

pneumoniae demonstrates notable phenotypic plasticity, allowing it to survive in various host environments

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Efekat je individualan i infuzija se ne primenjuje kao medicinski postupak za izbeljivanje koe, ve kao antioksidativna podrka

Although the body can produce the substance independently, the building blocks are often missing

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