Molecular Characterization of the Rare CFTR Mutation P67l as a Model for Genotype-specific Drug Development and Personalized Medicine in Cystic Fibrosis - ProQuest

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Molecular Characterization of the Rare CFTR Mutation P67l as a Model for Genotype-specific Drug Development and Personalized Medicine in Cystic Fibrosis

Sabusap, Carleen Mae Pomperada. The University of Alabama at Birmingham ProQuest Dissertations & Theses, 2018. 10830946.