Mutations in familial porphyria cutanea tarda: Two novel and two previously described for hepatoerythropoietic porphyria

Uroporphyrinogen decarboxylase (URO‐D) deficiency is responsible for two forms of genetic cutaneous porphyria: familial porphyria cutanea tarda (f‐PCT) and hepatoerythropoietic porphyria (HEP). The f‐PCT transmitted as an autosomal dominant trait, is characterized by photosensitive cutaneous lesions...

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