Whatley SD, Roberts AG, Llewellyn DH, Bennett CP, Garrett C, Elder GH (септембар 2000). „Non-erythroid form of acute intermittent porphyria caused by promoter and frameshift mutations distant from the coding sequence of exon 1 of the HMBS gene”. Human Genetics. 107 (3): 243—8. PMID11071386. S2CID40036227. doi:10.1007/s004390000356.CS1 одржавање: Формат датума (веза)
Solis C, Martinez-Bermejo A, Naidich TP, Kaufmann WE, Astrin KH, Bishop DF, Desnick RJ (новембар 2004). „Acute intermittent porphyria: studies of the severe homozygous dominant disease provides insights into the neurologic attacks in acute porphyrias”. Archives of Neurology. 61 (11): 1764—70. PMID15534187. doi:10.1001/archneur.61.11.1764.CS1 одржавање: Формат датума (веза)
Elder, G.; Harper, P.; Badminton, M.; Sandberg, S.; Deybach, J. C. (2013). „The incidence of inherited porphyrias in Europe”. Journal of Inherited Metabolic Disease. 36 (5): 849—857. PMID23114748. S2CID20442163. doi:10.1007/s10545-012-9544-4.
Stein, P.; Badminton, M.; Barth, J.; Rees, D.; Stewart, M. F.; British and Irish Porphyria Network (2013). „Best practice guidelines on clinical management of acute attacks of porphyria and their complications”. Annals of Clinical Biochemistry. 50 (Pt 3): 217—223. PMID23605132. S2CID206396284. doi:10.1177/0004563212474555.
Karim, Z.; Lyoumi, S.; Nicolas, G.; Deybach, J. C.; Gouya, L.; Puy, H. (2015). „Porphyrias: A 2015 update”. Clinics and Research in Hepatology and Gastroenterology. 39 (4): 412—425. PMID26142871. doi:10.1016/j.clinre.2015.05.009.
Whatley SD, Roberts AG, Llewellyn DH, Bennett CP, Garrett C, Elder GH (септембар 2000). „Non-erythroid form of acute intermittent porphyria caused by promoter and frameshift mutations distant from the coding sequence of exon 1 of the HMBS gene”. Human Genetics. 107 (3): 243—8. PMID11071386. S2CID40036227. doi:10.1007/s004390000356.CS1 одржавање: Формат датума (веза)
Solis C, Martinez-Bermejo A, Naidich TP, Kaufmann WE, Astrin KH, Bishop DF, Desnick RJ (новембар 2004). „Acute intermittent porphyria: studies of the severe homozygous dominant disease provides insights into the neurologic attacks in acute porphyrias”. Archives of Neurology. 61 (11): 1764—70. PMID15534187. doi:10.1001/archneur.61.11.1764.CS1 одржавање: Формат датума (веза)
Elder, G.; Harper, P.; Badminton, M.; Sandberg, S.; Deybach, J. C. (2013). „The incidence of inherited porphyrias in Europe”. Journal of Inherited Metabolic Disease. 36 (5): 849—857. PMID23114748. S2CID20442163. doi:10.1007/s10545-012-9544-4.
Stein, P.; Badminton, M.; Barth, J.; Rees, D.; Stewart, M. F.; British and Irish Porphyria Network (2013). „Best practice guidelines on clinical management of acute attacks of porphyria and their complications”. Annals of Clinical Biochemistry. 50 (Pt 3): 217—223. PMID23605132. S2CID206396284. doi:10.1177/0004563212474555.
Karim, Z.; Lyoumi, S.; Nicolas, G.; Deybach, J. C.; Gouya, L.; Puy, H. (2015). „Porphyrias: A 2015 update”. Clinics and Research in Hepatology and Gastroenterology. 39 (4): 412—425. PMID26142871. doi:10.1016/j.clinre.2015.05.009.
Whatley SD, Roberts AG, Llewellyn DH, Bennett CP, Garrett C, Elder GH (септембар 2000). „Non-erythroid form of acute intermittent porphyria caused by promoter and frameshift mutations distant from the coding sequence of exon 1 of the HMBS gene”. Human Genetics. 107 (3): 243—8. PMID11071386. S2CID40036227. doi:10.1007/s004390000356.CS1 одржавање: Формат датума (веза)
Elder, G.; Harper, P.; Badminton, M.; Sandberg, S.; Deybach, J. C. (2013). „The incidence of inherited porphyrias in Europe”. Journal of Inherited Metabolic Disease. 36 (5): 849—857. PMID23114748. S2CID20442163. doi:10.1007/s10545-012-9544-4.
Stein, P.; Badminton, M.; Barth, J.; Rees, D.; Stewart, M. F.; British and Irish Porphyria Network (2013). „Best practice guidelines on clinical management of acute attacks of porphyria and their complications”. Annals of Clinical Biochemistry. 50 (Pt 3): 217—223. PMID23605132. S2CID206396284. doi:10.1177/0004563212474555.