人富马酰乙酰乙酸水解酶（FAH）基因的Bg1II限制性片段长度多态性 - Suppr

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Bg1II RFLP for the human fumarylacetoacetate hydrolase (FAH) gene.

作者信息

Demers S I, Tanguay R M

机构信息

Ontogénèse et Génétique Moléculaire, Centre de Recherches du CHUL, Ste-Foy, Québec, Canada.

出版信息

Nucleic Acids Res. 1991 Apr 25;19(8):1965.

PMID:1674378

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC328157/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f08d/328157/9a9ea48b7ba4/nar00088-0222-a.jpg

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本文引用的文献

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):308-16.

Cloning and expression of the cDNA encoding human fumarylacetoacetate hydrolase, the enzyme deficient in hereditary tyrosinemia: assignment of the gene to chromosome 15.

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