{Reference Type}: Case Reports
{Title}: A rare case of porphyria cutanea tarda in a patient with a homozygous hereditary hemochromatosis gene H63D mutation in the setting of hereditary hemochromatosis.
{Author}: Banta J;Collins J;Kobayashi T;
{Journal}: JAAD Case Rep
{Volume}: 50
{Issue}: 0
{Year}: 2024 Aug
暂无{DOI}: 10.1016/j.jdcr.2024.05.023