Hereditary coproporphyria (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Hereditary coproporphyria" in English language version.

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Lourenco, Charles Marquez; Lee, Chul; Anderson, Karl E. (2012). "Disorders of Haem Biosynthesis". In Saudubray, Jean-Marie; van den Berghe, Georges; Walter, John H. (eds.). Inborn Metabolic Diseases: Diagnosis and Treatment (5th ed.). New York: Springer. pp. 521–532. ISBN 978-3-642-15719-6.

Schmitt, C.; Gouya, L.; Malonova, E.; Lamoril, J.; Camadro, J. M.; Flamme, M.; Rose, C.; Lyoumi, S.; Da Silva, V.; Boileau, C.; Grandchamp, B.; Beaumont, C.; Deybach, J. C.; Puy, H. (2005). "Mutations in human CPO gene predict clinical expression of either hepatic hereditary coproporphyria or erythropoietic harderoporphyria". Human Molecular Genetics. 14 (20): 3089–3098. doi:10.1093/hmg/ddi342. PMID 16159891.
Hasanoglu, A.; Balwani, M.; Kasapkara, Ç. D. S.; Ezgü, F. S.; Okur, İ.; Tümer, L.; Cakmak, A.; Nazarenko, I.; Yu, C.; Clavero, S.; Bishop, D. F.; Desnick, R. J. (2010). "Harderoporphyria due to homozygosity for coproporphyrinogen oxidase missense mutation H327R". Journal of Inherited Metabolic Disease. 34 (1): 225–231. doi:10.1007/s10545-010-9237-9. PMC 3091031. PMID 21103937.
Anderson, K. E.; Bloomer, J. R.; Bonkovsky, H. L.; Kushner, J. P.; Pierach, C. A.; Pimstone, N. R.; Desnick, R. J. (2005). "Recommendations for the diagnosis and treatment of the acute porphyrias". Annals of Internal Medicine. 142 (6): 439–450. doi:10.7326/0003-4819-142-6-200503150-00010. PMID 15767622. S2CID 36122555.
Ratnaike, S.; Blake, D. (1995). "The diagnosis and follow-up of porphyria". Pathology. 27 (2): 142–153. doi:10.1080/00313029500169762. PMID 7567142. S2CID 46438357.

Schmitt, C.; Gouya, L.; Malonova, E.; Lamoril, J.; Camadro, J. M.; Flamme, M.; Rose, C.; Lyoumi, S.; Da Silva, V.; Boileau, C.; Grandchamp, B.; Beaumont, C.; Deybach, J. C.; Puy, H. (2005). "Mutations in human CPO gene predict clinical expression of either hepatic hereditary coproporphyria or erythropoietic harderoporphyria". Human Molecular Genetics. 14 (20): 3089–3098. doi:10.1093/hmg/ddi342. PMID 16159891.
Hasanoglu, A.; Balwani, M.; Kasapkara, Ç. D. S.; Ezgü, F. S.; Okur, İ.; Tümer, L.; Cakmak, A.; Nazarenko, I.; Yu, C.; Clavero, S.; Bishop, D. F.; Desnick, R. J. (2010). "Harderoporphyria due to homozygosity for coproporphyrinogen oxidase missense mutation H327R". Journal of Inherited Metabolic Disease. 34 (1): 225–231. doi:10.1007/s10545-010-9237-9. PMC 3091031. PMID 21103937.
Anderson, K. E.; Bloomer, J. R.; Bonkovsky, H. L.; Kushner, J. P.; Pierach, C. A.; Pimstone, N. R.; Desnick, R. J. (2005). "Recommendations for the diagnosis and treatment of the acute porphyrias". Annals of Internal Medicine. 142 (6): 439–450. doi:10.7326/0003-4819-142-6-200503150-00010. PMID 15767622. S2CID 36122555.
Ratnaike, S.; Blake, D. (1995). "The diagnosis and follow-up of porphyria". Pathology. 27 (2): 142–153. doi:10.1080/00313029500169762. PMID 7567142. S2CID 46438357.

"Homo sapiens coproporphyrinogen oxidase, mRNA (cDNA clone MGC:19736 IMAGE:3607724), complete cds". US National Library of Medicine. Retrieved 2012-05-27.
Hasanoglu, A.; Balwani, M.; Kasapkara, Ç. D. S.; Ezgü, F. S.; Okur, İ.; Tümer, L.; Cakmak, A.; Nazarenko, I.; Yu, C.; Clavero, S.; Bishop, D. F.; Desnick, R. J. (2010). "Harderoporphyria due to homozygosity for coproporphyrinogen oxidase missense mutation H327R". Journal of Inherited Metabolic Disease. 34 (1): 225–231. doi:10.1007/s10545-010-9237-9. PMC 3091031. PMID 21103937.

"#121300 COPROPORPHYRIA, HEREDITARY; HCP". Johns Hopkins University. Retrieved 2012-05-27.

"Tests for Porphyria Diagnosis". National Porphyria Foundation. Archived from the original on 2014-03-20. Retrieved 2012-05-28.

Anderson, K. E.; Bloomer, J. R.; Bonkovsky, H. L.; Kushner, J. P.; Pierach, C. A.; Pimstone, N. R.; Desnick, R. J. (2005). "Recommendations for the diagnosis and treatment of the acute porphyrias". Annals of Internal Medicine. 142 (6): 439–450. doi:10.7326/0003-4819-142-6-200503150-00010. PMID 15767622. S2CID 36122555.
Ratnaike, S.; Blake, D. (1995). "The diagnosis and follow-up of porphyria". Pathology. 27 (2): 142–153. doi:10.1080/00313029500169762. PMID 7567142. S2CID 46438357.

"Tests for Porphyria Diagnosis". National Porphyria Foundation. Archived from the original on 2014-03-20. Retrieved 2012-05-28.