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Hereditary Tyrosinemia
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Hereditary Tyrosinemia

Hereditary tyrosinemia type 1 (HT1), the most severe inborn error of the tyrosine degradation pathway, is due to a deficiency in fumarylacetoacetate hydrolase (FAH).
Undertitel
Pathogenesis, Screening and Management
Upplaga
1st ed. 2017
ISBN
9783319557793
Språk
Engelska
Vikt
446 gram
Utgivningsdatum
2017-08-10
Sidor
247