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Page 1
A novel missense mutation (Y89C) in exon 3 of the CFTR (ABCC7) gene in a young male.
Padoan R, Costantini D, Russo MC, Ambrosioni A, Fiori S, Prandoni S, Cantù-Rajnoldi A, Seia M, Giunta A. Padoan R, et al. Among authors: prandoni s. Hum Mutat. 2000 May;15(5):486. doi: 10.1002/(SICI)1098-1004(200005)15:5<486::AID-HUMU25>3.0.CO;2-S. Hum Mutat. 2000. PMID: 10790225 No abstract available.
Bartter syndrome type 3: an unusual cause of nephrolithiasis.
Colussi G, De Ferrari ME, Tedeschi S, Prandoni S, Syrén ML, Civati G. Colussi G, et al. Among authors: prandoni s. Nephrol Dial Transplant. 2002 Mar;17(3):521-3. doi: 10.1093/ndt/17.3.521. Nephrol Dial Transplant. 2002. PMID: 11865110 No abstract available.