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Coexistence of hereditary coproporphyria and epilepsy: Coproporphyrinogen oxidase deficiency in liver and kidney

✍ Scribed by M. Doss; R. Tiepermann; K. -H. Pflüger


Book ID
104717698
Publisher
Springer
Year
1981
Tongue
English
Weight
516 KB
Volume
226
Category
Article
ISSN
0340-5354

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## Communicated by Peter Byers Hereditary coproporphyria (HC) is an acute hepatic porphyria with autosomal dominant inheritance caused by deficient activity of coproporphyrinogen III oxidase (CPO). Clinical manifestations of the disease are characterized by acute attacks of neurological dysfunctio

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