Congenital erythropoietic porphyria: Insight into the molecular basis of the disease
Congenital Erythropoietic Porphyria (CEP) is a rare inborn error of metabolism charectorised by a deficiency of UROS III enzyme, an important enzyme in the heme biosythetic pathway. It is an autosomal recessive disease and only around 200 cases have been charectorised so far. The clinical presentati...
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| Автори: | , , , |
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| Формат: | Книга |
| Опубліковано: |
Wolters Kluwer Medknow Publications,
2016-01-01T00:00:00Z.
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Connect to this object online.3rd Floor Main Library
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A1234.567 |
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| Примірник 1 | Доступно |