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Hereditary Tyrosinemia
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Hereditary Tyrosinemia

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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).
Undertitel
Pathogenesis, Screening and Management
Upplaga
Softcover Reprint of the Original 1st 2017 ed.
ISBN
9783319857459
Språk
Engelska
Vikt
310 gram
Utgivningsdatum
2018-08-12
Sidor
247