These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
2. Porphyria cutanea tarda as the most common porphyria. Bulat V; Lugović L; Situm M; Buljan M; Bradić L Acta Dermatovenerol Croat; 2007; 15(4):254-63. PubMed ID: 18093456 [TBL] [Abstract][Full Text] [Related]
3. Mutations in familial porphyria cutanea tarda: two novel and two previously described for hepatoerythropoietic porphyria. Mendez M; Rossetti MV; De Siervi A; del Carmen Batlle AM; Parera V Hum Mutat; 2000 Sep; 16(3):269-70. PubMed ID: 10980536 [TBL] [Abstract][Full Text] [Related]
4. A mutation (G281E) of the human uroporphyrinogen decarboxylase gene causes both hepatoerythropoietic porphyria and overt familial porphyria cutanea tarda: biochemical and genetic studies on Spanish patients. Roberts AG; Elder GH; De Salamanca RE; Herrero C; Lecha M; Mascaro JM J Invest Dermatol; 1995 Apr; 104(4):500-2. PubMed ID: 7706766 [TBL] [Abstract][Full Text] [Related]
16. [Enzymatic and molecular studies in a case of hepato-erythropoietic porphyria. Homozygote form of type familial cutaneous porphyria]. de Verneuil H; Moreau-Gaudry F; Laradi S; Cruces MJ; de la Torre C; Aris LF Arch Fr Pediatr; 1992 Dec; 49(10):907-11. PubMed ID: 1363904 [TBL] [Abstract][Full Text] [Related]