Hereditary Tyrosinemia: Pathogenesis, Screening and Management - Advances in Experimental Medicine and Biology - - Books - Springer International Publishing AG - 9783319557793 - August 10, 2017
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Hereditary Tyrosinemia: Pathogenesis, Screening and Management - Advances in Experimental Medicine and Biology 1st ed. 2017 edition

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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).

247 pages, 36 Illustrations, color; 17 Illustrations, black and white; XV, 247 p. 53 illus., 36 illu

Media Books     Hardcover Book   (Book with hard spine and cover)
Released August 10, 2017
ISBN13 9783319557793
Publishers Springer International Publishing AG
Pages 247
Dimensions 150 × 220 × 20 mm   ·   700 g
Language German  
Editor Tanguay, Robert M.

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