The inherited enzymatic defect in porphyria variegata
Author:
Publisher
Springer Science and Business Media LLC
Subject
Genetics (clinical),Genetics
Link
http://link.springer.com/content/pdf/10.1007/BF00282829.pdf
Reference17 articles.
1. Becker DM, Viljoen JD, Katz J, Kramer S (1977) Reduced ferrochelatase activity: a defect common to porphyria variegata and protoporphyria. Br J Haematol 36:171–179
2. Bonkowsky HL, Bloomer JR, Ebert PS, Mahoney MJ (1975) Heme synthetase deficiency in human protoporphyria. J Clin Invest 56: 1139–1148
3. Bottomley SS (1968) Characterization and measurement of heme synthetase in normal human bone marrow. Blood 31:314–322
4. Boyum A (1968) Separation of leucocytes from blood and bone marrow. Scand J Clin Lab Invest 21: (Suppl) 97
5. Brenner DA, Bloomer JR (1980a) A fluorometric assay for measurement of protoporphyrinogen oxidase activity in mammalian tissue. Clin Chim Acta 100:259–769
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