High Quality Content by WIKIPEDIA articles! ?F508 (delta-F508) is a specific mutation within the human genome. The mutation is a deletion of three base pairs at position 508 in the nucleotide sequence of a protein called the cystic fibrosis transmembrane conductance regulator (CFTR). The deletion prevents the codon for phenylalanine (F) from obtaining its normal position. Having two copies of this mutation, inherited from both parents, is the leading cause of cystic fibrosis (CF).

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