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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).
Undertittel
Pathogenesis, Screening and Management
Opplag
1st ed. 2017
ISBN
9783319557793
Språk
Engelsk
Vekt
446 gram
Utgivelsesdato
10.8.2017
Antall sider
247