Different molecular basis for fumarylacetoacetate hydrolase deficiency in the two clinical forms of hereditary tyrosinemia (type I) (Q24676845)
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scientific article
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Different molecular basis for fumarylacetoacetate hydrolase deficiency in the two clinical forms of hereditary tyrosinemia (type I) |
scientific article |
Statements
Different molecular basis for fumarylacetoacetate hydrolase deficiency in the two clinical forms of hereditary tyrosinemia (type I) (English)
Tanguay RM
Valet JP
Lescault A
Duband JL
Laberge C
Lettre F
1 August 1990
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