Walking the ethical highwire: Genetic sc
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RenΓ© Romero; Joel E. Lavine
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Article
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1995
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John Wiley and Sons
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English
β 360 KB
Background. Hereditary tyrosinemia type I is an autosomal recessive inborn error of metabolism caused by a deficiency of the enzyme fumarylacetoacetate hydrolase. The disorder clusters in the Saguenay-Lac-St.-Jean area of Quebec. In this region, 1 of 1846 newborns is affected and 1 of every 22 perso