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Tantis, I

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doi:10.1001/jama.2021.2909 Dagres N, Varounis C, Iliodromitis EK, Lekakis JP, Rallidis LS, Anastasiou-Nana M

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While many of these mutations lead to the loss of transport function, the most common mutation, a deletion of phenylalanine (F) at residue 508 (F508), causes cystic fibrosis due to its rapid degradation at the ER (1)

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