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CF is caused by recessive mutations in the cystic fibrosis transmembrane conductance regulator ( CFTR ) gene that then lead to incomplete transport to the membrane or malfunctioning of the CFTR protein (Van Goor et al., 2009
cyanocobalamin
Supply:6 Months
Administration : Les capsules sont avalées entieres sans masticage dans les protocoles d'auto-administration
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