. . . . . . . "[Analysis of TFRC1 genotypes and HFE gene mutations in French porphyria cutanea tarda (sPCT) patients revealed that, independently from HFE gene mutations, an association was found between the IVS4+198 T allele in the TFRC1 gene and sPCT patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en . . . . . "2009-03-31"^^ . . "Gene-disease associations inferred from text-mining the literature."@en . "DisGeNET evidence - LITERATURE"@en . "2017-10-17T13:16:38+02:00"^^ . . . . . . . . . . . "v5.0.0.0" . "v5.0.0" .