Hereditary Tyrosinemia
Springer International Publishing AG, 2018
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Hereditary tyrosinemia type 1 (HT1), the most severe inborn error of the tyrosine degradation pathway, is due to a deficiency in fumarylacetoacetate hydrolase (FAH).
- ISBN-13
- 9783319857459
- ISBN-10
- 3319857452
- Publisher
- Springer International Publishing AG
- Year
- 2018
- Publication date
- 2018-08-12
- Pages
- 247
- Dimensions
- 254x178x