MAKE A MEME View Large Image CFTRdel4.png The ΔF508 human genome mutation is characterized by the deletion of three base pairs in the CFTR nucleotide sequence causing the loss of the amino acid phenylalanine located at position 508 Oak Ridge National Laboratory Human ...
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Keywords: CFTRdel4.png The ΔF508 human genome mutation is characterized by the deletion of three base pairs in the CFTR nucleotide sequence causing the loss of the amino acid phenylalanine located at position 508 Oak Ridge National Laboratory Human Genome Project website U S federal government source PD-USGov Genetic diseases and disorders Original upload log wikitable - - 2008-07-11 21 12 38 275 × 230 6692 bytes Twohoos <nowiki> The ΔF508 human genome mutation is characterized by the deletion of three base pairs in the CFTR nucleotide sequence causing the loss of the amino acid phenylalanine located at position 508 So</nowiki>
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