Iron status and HFE mutations in first-degree relatives of patients with sporadic porphyria cutanea tarda, in a Mediterranean area

HARPER, P.
FLODERUS, Y.
HOLMSTRÖM, P.
EGGERTSEN, G.
GÅFVELS, M.

¹Porphyria Centre Sweden, Division of Inherited Metabolic Diseases, Stockholm, Sweden
²Division of Clinical Chemistry, Department of Laboratory Medicine, Karolinska Institute, Karolinska University Hospital, SE-141 86 Stockholm, Sweden

Correspondence: Dr Pauline Harper, Porphyria Centre Sweden, Division of Inherited Metabolic Diseases, Karolinska Institute, Karolinska University Hospital Huddinge 141 86 Stockholm Sweden. (Tel.: +46 8585 82787; fax: +46 858582760; e-mail: [email protected]).

Journal of Internal Medicine 257(4):p 393, April 2005.