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Characterization of a novel 21-kb deletion, CFTRdele2,3(21 kb), in the CFTR gene: a cystic fibrosis mutation of Slavic origin common in Central and East Europe

FibrosisMendelian DisorderGenetic DisorderMedicineGeneticsPathogenesisPathologyPulmonary FibrosisMolecular GeneticsCftr GeneDisease Gene IdentificationMedical GeneticsSlavic OriginCystic Fibrosis Mutation