Deficiency of hepatic coproporphyrinogen oxidase in hereditary coproporphyria
- PMID: 712737
- PMCID: PMC1436210
- DOI: 10.1177/014107687807101018
Deficiency of hepatic coproporphyrinogen oxidase in hereditary coproporphyria
Similar articles
-
Coexistence of hereditary coproporphyria and epilepsy: coproporphyrinogen oxidase deficiency in liver and kidney.J Neurol. 1981;226(1):25-33. doi: 10.1007/BF00313315. J Neurol. 1981. PMID: 6181213 No abstract available.
-
[Demonstration of hereditary enzyme defect in coproporphyria].Nouv Presse Med. 1977 Apr 30;6(18):1537-9. Nouv Presse Med. 1977. PMID: 866144 French.
-
Coproporphyrinogen-oxidase deficiency in hereditary coproporphyria.Lancet. 1977 Jan 15;1(8003):140. doi: 10.1016/s0140-6736(77)91725-1. Lancet. 1977. PMID: 64669 No abstract available.
-
Recent advances in the identification of enzyme deficiencies in the porphyrias.Br J Dermatol. 1983 Jun;108(6):729-34. doi: 10.1111/j.1365-2133.1983.tb01088.x. Br J Dermatol. 1983. PMID: 6344903 Review. No abstract available.
-
A review of the enzymic errors in the various porphyrias.Scand J Clin Lab Invest. 1985 Jun;45(4):291-301. doi: 10.3109/00365518509161010. Scand J Clin Lab Invest. 1985. PMID: 3892647 Review. No abstract available.
Cited by
-
Characterization of mutations in the CPO gene in British patients demonstrates absence of genotype-phenotype correlation and identifies relationship between hereditary coproporphyria and harderoporphyria.Am J Hum Genet. 2001 May;68(5):1130-8. doi: 10.1086/320118. Epub 2001 Apr 16. Am J Hum Genet. 2001. PMID: 11309681 Free PMC article.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources