Different molecular basis for fumarylacetoacetate hydrolase deficiency in the two clinical forms of hereditary tyrosinemia (type I) (Q24676845)
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Current Data About Different molecular basis for fumarylacetoacetate hydrolase deficiency in the two clinical forms of hereditary tyrosinemia (type I)
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(P1476) "Different molecular basis for fumarylacetoacetate hydrolase deficiency in the two clinical forms of hereditary tyrosinemia (type I)" (language: en)
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(P2093) Tanguay RM
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Valet JP
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Lescault A
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Duband JL
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Laberge C
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Lettre F
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Plante M
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