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Cystic fibrosis arises from mutations in the gene CFTR, also known as cystic fibrosis transmembrane conductance regulator. a What is the function of the CFTR protein? b The delta -F508 mutation, which is the most common allele linked to cystic fibrosis, results from the loss of a single codon in the CFTR gene. How does this affect the length of the coding sequence (i.e., at the nucleotide level), and the protein sequence (i.e., at the amino acid level)?