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Bialleleic PKD1 mutations underlie early-onset autosomal dominant polycystic kidney disease in Saudi Arabian families

Mendelian DisorderGenetic DisorderMedicineGeneticsInherited Metabolic DiseaseGenetic EpidemiologyRenal PathologyPathologyKidney FailureDisease Gene IdentificationSaudi Arabian FamiliesChronic Kidney DiseaseNephrologyKidney Research