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J Cutan Pathol 42(5):308-317, 2015

g-glutamyltransferase The autosomal recessive disorder known as cystic brosis (CF) is due to mutations in the cystic brosis transmembrane regulator protein (CFTR), leading to an intrinsic defect in the CFTR-mediated Cl 2 secretory pathway and unregulated Na 1 absorption

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This is due to cyclophosphamides suppression of both white and red blood cells