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. 1991 Mar 25;19(6):1352. doi: 10.1093/nar/19.6.1352-a

TaqI RFLP for the human fumarylacetoacetate hydrolase (FAH) gene

Sylvie I Demers ¹, Daniel Phaneuf ¹, Robert M Tanguay ¹

PMCID: PMC333878 PMID: 1674367

Abstract

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

Tanguay R. M., Valet J. P., Lescault A., Duband J. L., Laberge C., Lettre F., Plante M. Different molecular basis for fumarylacetoacetate hydrolase deficiency in the two clinical forms of hereditary tyrosinemia (type I). Am J Hum Genet. 1990 Aug;47(2):308–316. [PMC free article] [PubMed] [Google Scholar]

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