More than 2000 mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) have been defined that confer a number of molecular cells' organic and functional phenotypes.
Everybody has two copies of the CFTR gene, and there ought to be mutations in both copies to purpose CF. more than 1, 700mutations of the CFTR gene had been identified.
Mutations in the gene encoding the cystic fibrosis transmembrane conductance regulator (CFTR) anion channel motivate the autosomal recessive disease, cystic fibrosis (CF).
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