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13. Seven novel point mutations in the uroporphyrinogen decarboxylase (UROD) gene in patients with familial porphyria cutanea tarda (f-PCT). Cappellini MD; Martinez di Montemuros F; Tavazzi D; Fargion S; Pizzuti A; Comino A; Cainelli T; Fiorelli G Hum Mutat; 2001 Apr; 17(4):350. PubMed ID: 11295834 [TBL] [Abstract][Full Text] [Related]
14. Screening for mutations in the uroporphyrinogen decarboxylase gene using denaturing gradient gel electrophoresis. Identification and characterization of six novel mutations associated with familial PCT. Christiansen L; Ged C; Hombrados I; Brons-Poulsen J; Fontanellas A; de Verneuil H; Hørder M; Petersen NE Hum Mutat; 1999; 14(3):222-32. PubMed ID: 10477430 [TBL] [Abstract][Full Text] [Related]
15. [Hepatitis C, hemochromatosis and porphyria cutanea tarda]. Teubner A; Richter M; Schuppan D; Köstler E; Stölzel U Dtsch Med Wochenschr; 2006 Mar; 131(13):691-5. PubMed ID: 16555178 [TBL] [Abstract][Full Text] [Related]
16. [Porphyria cutanea tarda is the most common type of porphyria. Medical control is a team work]. Harper P; Thunell S; Hultcrantz R; Ros AM; Wennersten G Lakartidningen; 1998 Jul; 95(28-29):3195-9. PubMed ID: 9700265 [TBL] [Abstract][Full Text] [Related]