TLS Online TPP Program

#Question id: 31150


The most common CFTR mutation is a deletion of a phenylalanine at position 508 in the protein sequence. This mutation prevents:

#Unit 2. Cellular Organization
  1. Normal transport of CFTR by blocking its packaging into COPI vesicles
  2. Normal transport of CFTR by blocking its packaging into COPII vesicles
  3. Normal folding of CFTR by blocking chaperons' activity
  4. Normal functioning of CFTR by blocking its channel formation