Hereditary Tyrosinemia: Pathogenesis, Screening and Management - Advances in Experimental Medicine and Biology - - Books - Springer International Publishing AG - 9783319857459 - August 12, 2018
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Hereditary Tyrosinemia: Pathogenesis, Screening and Management - Advances in Experimental Medicine and Biology Softcover Reprint of the Original 1st 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     Paperback Book   (Book with soft cover and glued back)
Released August 12, 2018
ISBN13 9783319857459
Publishers Springer International Publishing AG
Pages 247
Dimensions 150 × 220 × 10 mm   ·   503 g
Language German  
Editor Tanguay, Robert M.

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