Encyclopedia : F : F5 : F50 (6 articles)

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ΔF508
ΔF508 is a specific mutation within the human genome. The mutation--a deletion of three base pairs which form the codon for phenylalanine (F) at the 508 position--prevents a protein called the cystic fibrosis transmembrane conductance regulator (CFTR) from obtaining its normal position. Having tw..

 

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