人类富马酰乙酰乙酸水解酶（FAH）基因中的MspI限制性片段长度多态性 - Suppr | 超能文献

MspI RFLP in 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 Dec 25;19(24):6971. doi: 10.1093/nar/19.24.6971.

DOI:10.1093/nar/19.24.6971

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC329360/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/684f/329360/9aa408d0b1eb/nar00104-0281-a.jpg

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本文引用的文献

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Different molecular basis for fumarylacetoacetate hydrolase deficiency in the two clinical forms of hereditary tyrosinemia (type I).遗传性酪氨酸血症（I型）两种临床形式中富马酰乙酰乙酸水解酶缺乏的不同分子基础。

Am J Hum Genet. 1990 Aug;47(2):308-16.

2

Cloning and expression of the cDNA encoding human fumarylacetoacetate hydrolase, the enzyme deficient in hereditary tyrosinemia: assignment of the gene to chromosome 15.编码人富马酰乙酰乙酸水解酶（遗传性酪氨酸血症中缺乏的酶）的cDNA的克隆与表达：该基因定位于15号染色体

Am J Hum Genet. 1991 Mar;48(3):525-35.