Letter to the Editor regarding the article “Porphyria cutanea tarda: A novel mutation” by Patil R et al. in doi:10.1016/j.phoj.2016.04.001
Author:
Publisher
Elsevier BV
Subject
Oncology,Hematology,Pediatrics, Perinatology, and Child Health
Reference14 articles.
1. Uroporphyrinogen decarboxylase;Elder;J Bioenerg Biomembr,1995
2. Modern diagnosis and management of the porphyrias;Sassa;Br J Haematol,2006
3. Hepatoerythropoietic porphyria: a new uroporphyrinogen decarboxylase defect or homozygous porphyria cutanea tarda?;Elder;Lancet,1981
4. A mutation (G281E) of the human uroporphyrinogen decarboxylase gene causes both hepatoerythropoietic porphyria and overt familial porphyria cutanea tarda: biochemical and genetic studies on Spanish patients;Roberts;J Invest Dermatol,1995
5. Uroporphyrinogen decarboxylase. complete human gene sequence and molecular study of three families with hepatoerythropoietic porphyria;Moran-Jimenez;Am J Hum Genet,1996
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