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Hereditary Tyrosinemia: Pathogenesis, Screening and Management - Advances in Experimental Medicine and Biology Softcover Reprint of the Original 1st 2017 edition
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Hereditary Tyrosinemia: Pathogenesis, Screening and Management - Advances in Experimental Medicine and Biology
Hereditary tyrosinemia type 1 (HT1), the most severe inborn error of the tyrosine degradation pathway, is due to a deficiency in fumarylacetoacetate hydrolase (FAH).
247 pages, 36 Illustrations, color; 17 Illustrations, black and white; XV, 247 p. 53 illus., 36 illu
| Mediji | Grāmatas Paperback Book (Grāmata ar mīksto vāku un līmēto muguru) |
| Izlaists | 2018. gada 12. augusts |
| ISBN13 | 9783319857459 |
| Izdevēji | Springer International Publishing AG |
| Lapas | 247 |
| Izmēri | 150 × 220 × 10 mm · 503 g |
| Valoda | Vācu |
| Redaktors | Tanguay, Robert M. |
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