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Brindha, S
Among all the mutations, the most common is named F508del, which, through the deletion of phenylalanine at position 508 of the CFTR protein (O'Sullivan and Freedman, 2009
Bernardeau et al., 2008)
In a separate arm of investigation, another 12 patients with cirrhosis received GSH 200 mg/d im without producing any difference in biochemical parameters
