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Biology, 27.07.2019 11:30 violetagamez2

The most commonly occurring mutation in people with cystic fibrosis is a deletion of a single codon. this results in the most commonly occurring mutation in people with cystic fibrosis is a deletion of a single codon. this results in a frameshift mutation a polypeptide missing an amino acid a nucleotide mismatch a base-pair substitution a nonsense mutation

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