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- W2415628531 abstract "During the last 10 years our knowledge concerning the basis defect in porphyrias has increased so that a better genetic family advice. The following basis defects were found: 1. Uroporphyrinogen-III-cosynthetase in porphyria erythropoetica congenita, 2. haem-synthetase in protoporphyria erythropoetica, 3. uroporphyrinogen-1-synthetase in porphyria acuta intermittens, 4. uroporphyrinogen-carboxylase in porphyria cutanea tarda. According to this in porphyria cutanea tarda a genetic defect is supposed, which leads to the disease in connection with the environmental factors. On the basis of the biochemical findings a better understanding of the heredity is possible which is discussed in detail." @default.
- W2415628531 created "2016-06-24" @default.
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- W2415628531 date "1981-06-01" @default.
- W2415628531 modified "2023-09-23" @default.
- W2415628531 title "[Porphyrin diseases with particular emphasis on hereditary]." @default.
- W2415628531 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/7303763" @default.
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