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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
Softcover Reprint of the Original 1st 2017 ed.
ISBN
9783319857459
Språk
Engelsk
Vekt
310 gram
Utgivelsesdato
12.8.2018
Antall sider
247