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Published in 2021 at "Membranes"
DOI: 10.3390/membranes11110804
Abstract: Cystic fibrosis is a hereditary disease that mainly affects secretory organs in humans. It is caused by mutations in the gene encoding CFTR with the most common phenylalanine deletion at position 508. CFTR is an…
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Keywords:
cftr;
intracellular compartments;
distribution role;
role cftr ... See more keywords