Publication | Closed Access
The Molecular Basis of Disease Variability among Cystic Fibrosis Patients Carrying the 3849+10 kb C→T Mutation
88
Citations
25
References
1998
Year
Genetic DisorderMedicineGeneticsPathogenesisGenetic EpidemiologyCystic Fibrosis PatientsPathologyKb C→t MutationDisease Gene IdentificationMolecular MedicineMonogenic DisordersPublic HealthMolecular DiagnosticsDisease VariabilityClinical Genetics
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