A rare case of porphyria cutanea tarda in a patient with a homozygous hereditary hemochromatosis gene H63D mutation in the setting of hereditary hemochromatosis
| Published in: | JAAD Case Reports |
|---|---|
| Main Authors: | , , |
| Format: | Article |
| Language: | English |
| Published: |
Elsevier
2024-08-01
|
| Subjects: | |
| Online Access: | http://www.sciencedirect.com/science/article/pii/S2352512624002042 |
