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Hereditary Tyrosinemia: Pathogenesis, Screening and Management - Advances in Experimental Medicine and Biology 1st ed. 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 Hardcover Book (Grāmata ar cieto muguriņu un vāku) |
| Izlaists | 2017. gada 10. augusts |
| ISBN13 | 9783319557793 |
| Izdevēji | Springer International Publishing AG |
| Lapas | 247 |
| Izmēri | 150 × 220 × 20 mm · 700 g |
| Valoda | Vācu |
| Redaktors | Tanguay, Robert M. |
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