Hepatoerythropoietic Porphyria Caused by a Novel Homoallelic Mutation in Uroporphyrinogen Decarboxylase Gene in Egyptian Patients Cited by

Fol. Biol. 2015, 61, 219-226

https://doi.org/10.14712/fb2015061060219

Hepatoerythropoietic Porphyria Caused by a Novel Homoallelic Mutation in Uroporphyrinogen Decarboxylase Gene in Egyptian Patients

M. S. Farrag¹, I. Mikula¹, E. Richard^2,3, V. Saudek⁴, H. De Verneuil^2,3, Pavel Martásek¹

¹Department of Paediatrics and Adolescent Medicine, First Faculty of Medicine, Charles University in Prague and General University Hospital in Prague, Czech Republic
²INSERM U1035, Bordeaux, France
³University of Bordeaux, Bordeaux, France
⁴University of Cambridge Metabolic Research Laboratories and MRC Metabolic Diseases Unit, Wellcome-MRC Institute of Metabolic Science, Addenbrooke’s Hospital, Cambridge, UK

Received July 2015
Accepted August 2015

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