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5. Fumarylacetoacetate hydrolase knockout rabbit model for hereditary tyrosinemia type 1

Fumarylacetoacetate hydrolase knockout rabbit model for hereditary tyrosinemia type 1

来源 :第九届广州国际干细胞与再生医学论坛暨第五届中国再生细胞生物学年会 | 被引量 : 0次 | 上传用户：uspjxt

【摘 要】

：

Hereditary tyrosinemia type 1(HT1)is a severe human autosomal recessive disorder caused by the deficiency of fumarylacetoacetate hydroxylase(FAH),an enzyme catalyzing the last step in the tyrosine deg

【作 者】

：

Li Li Liangxue Lai 

【机 构】

：

Guangzhou Institutes of Biomedicine and Health,Chinese Academy of Sciences,China

【出 处】

：

第九届广州国际干细胞与再生医学论坛暨第五届中国再生细胞生物学年会

【发表日期】

：

2016年5期

【关键词】

：

Hereditary tyrosinemia type 1 Fumarylacetoacetate hydroxylase Genetically engine 

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　　Hereditary tyrosinemia type 1(HT1)is a severe human autosomal recessive disorder caused by the deficiency of fumarylacetoacetate hydroxylase(FAH),an enzyme catalyzing the last step in the tyrosine degradation pathway.

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