Normal Function of the Cystic Fibrosis Conductance Regulator Protein Can Be Associated with Homozygous ΔF508 Mutation

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Identification of the Cystic Fibrosis Gene: Genetic Analysis

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Defective intracellular transport and processing of CFTR is the molecular basis of most cystic fibrosis

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Long-Term Study of One Hundred Five Patients with Cystic Fibrosis

Harry Shwachman · A M A Journal of Diseases of Children · 1958 · 1K citations

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The Relation between Genotype and Phenotype in Cystic Fibrosis — Analysis of the Most Common Mutation (ΔF₅₀₈)

Eitan Kerem, Mary Corey, Batsheva Kerem et al. · New England Journal of Medicine · 1990 · 732 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14