Genetic, Metabolic, and Biochemical Aspects of the Porphyrias
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Publisher
Springer US
Link
http://link.springer.com/content/pdf/10.1007/978-1-4615-8303-5_3.pdf
Reference517 articles.
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3. Amoroso, E. C., Loosmore, R. M., Rimington, C., and Tooth, B. E., 1957, Congenital porphyria in bovines: First living cases in Britain, Nature 180:230–231.
4. Anderson, K. E., Sassa, S., Peterson, C.M., and Kappas, A., 1977, Increased erythrocyte uroporphyrinogen-I-synthetase, δ-aminolevulinic acid dehydratase and protoporphyrin in hemolytic anemias, Am. J. Med. 63:359–364.
5. Anderson, K. E., Bradlow, H. L., Sassa, S., and Kappas, A., 1979, Studies in porphyria VIII. Relationship of the 5α-reductase metabolism of steroid hormones to clinical expression of the genetic defect in acute intermittent porphyria, Am. J. Med. 66:644–650.
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