HuGE Literature Finder
Records
1
-
3
Porphyria cutanea tarda, hepatitis C, uroporphyrinogen decarboxylase and mutations of HFE gene. A case-control study. Dermatology (Basel, Switzerland) 2009 218 (1): 15-21. Cribier Bernard, Chiaverini Christine, Dali-Youcef Nassim, Schmitt Michèle, Grima Michèle, Hirth Christine, Lacour Jean-Philippe, Chosidow Olivi |
Hemochromatosis (HFE) and transferrin receptor-1 (TFRC1) genes in sporadic porphyria cutanea tarda (sPCT). Cellular and molecular biology (Noisy-le-Grand, France) 2002 Feb 48 (1): 33-41. Lamoril Jér?me, Andant Christophe, Gouya Laurent, Malonova Eva, Grandchamp Bernard, Martásek Pavel, Deybac Jean-Charles, Puy Her |
CYP1A2*1F and GSTM1 alleles are associated with susceptibility to porphyria cutanea tarda. Molecular medicine (Cambridge, Mass.) 0 17 (3-4): 241-7. Wickliffe Jeffrey K, Abdel-Rahman Sherif Z, Lee Chul, Kormos-Hallberg Csilla, Sood Gagan, Rondelli Catherine M, Grady James J, Desnick Robert J, Anderson Karl |
- Page last reviewed:Feb 1, 2023
- Page last updated:Mar 30, 2023
- Content source: