Hepatoerythropoietic Porphyria.
Rudnick S, Phillips J, Bonkovsky H; Porphyrias Consortium of the Rare Diseases Clinical Research Network.
2013 Oct 31 [updated 2022 Dec 22]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024.
Porphyria Diagnostics-Part 1: A Brief Overview of the Porphyrias.
Ramanujam VS, Anderson KE.
Curr Protoc Hum Genet. 2015 Jul 1;86:17.20.1-17.20.26. doi: 10.1002/0471142905.hg1720s86.
Hepatoerythropoietic porphyria.
Bundino S, Topi GC, Zina AM, D'Allessandro Gandolfo L.
Pediatr Dermatol. 1987 Nov;4(3):229-33. doi: 10.1111/j.1525-1470.1987.tb00784.x.
Hepatoerythropoietic porphyria.
Czarnecki DB.
Arch Dermatol. 1980 Mar;116(3):307-11.
Porphyria Cutanea Tarda.
Shah A, Bhatt H.
2023 Apr 17. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2024 Jan–.
Hepatoerythropoietic porphyria: relationship with familial porphyria cutanea tarda.
Castaño Suárez E, Zamarro Sanz O, Guerra Tapia A, Enríquez de Salamanca R.
Dermatology. 1996;193(4):332-5. doi: 10.1159/000246284.
Porphyria cutanea tarda and hepatoerythropoietic porphyria: Identification of 19 novel uroporphyrinogen III decarboxylase mutations.
Weiss Y, Chen B, Yasuda M, Nazarenko I, Anderson KE, Desnick RJ.
Mol Genet Metab. 2019 Nov;128(3):363-366. doi: 10.1016/j.ymgme.2018.11.013. Epub 2018 Nov 28.
Hepatoerythropoietic porphyria: neuroimaging findings.
Berenguer J, Blasco J, Cardenal C, Pujol T, Cruces Prado MJ, Herrero C, Mascaró JM, de la Torre C, Mercader JM.
AJNR Am J Neuroradiol. 1997 Sep;18(8):1557-60.
Hepatoerythropoietic Porphyria Caused by a Novel Homoallelic Mutation in Uroporphyrinogen Decarboxylase Gene in Egyptian Patients.
Farrag MS, Mikula I, Richard E, Saudek V, De Verneuil H, Martásek P.
Folia Biol (Praha). 2015;61(6):219-26.
[Hepatoerythropoietic porphyria].
Kondo M, Yano Y.
Ryoikibetsu Shokogun Shirizu. 1998;(19 Pt 2):149-51.
