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Functional characterization of lon channels with a crucial role in cystic fibro...

Tese de doutoramento, Bioquímica (Genética Molecular), Universidade de Lisboa, Faculdade de Ciências, 2011 ; Cystic Fibrosis (CF) is a genetic disease leading to a progressive major pulmonary dysfunction and caused by mutations in the gene encoding the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) protein, which, in CF, has impaired function and/or expression. CFTR is an ABC-transporter expressed ...