A rare case of porphyria cutanea tarda in a patient with a homozygous hereditary hemochromatosis gene H63D mutation in the setting of hereditary hemochromatosis
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| Main Authors: | , , |
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| Format: | Book |
| Published: |
Elsevier,
2024-08-01T00:00:00Z.
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| Subjects: | |
| Online Access: | Connect to this object online. |
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| Item Description: | 2352-5126 10.1016/j.jdcr.2024.05.023 |
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