人不同组织中β-半乳糖苷酶A和B的变异性。 - Suppr

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超能文献

Variability of -galactosidase A and B in different tissues of man.

作者信息

Beutler E, Guinto E, Kuhl W

出版信息

Am J Hum Genet. 1973 Jan;25(1):42-6.

PMID:4346241

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1762225/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0717/1762225/66b81f5a867e/ajhg00446-0045-a.jpg

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本文引用的文献

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FEBS Lett. 1971 Feb 12;13(1):68-72. doi: 10.1016/0014-5793(71)80667-1.

Fabry's disease: alpha-galactosidase deficiency.法布里病：α-半乳糖苷酶缺乏症。

Science. 1970 Feb 27;167(3922):1268-9. doi: 10.1126/science.167.3922.1268.

Fabry's disease: structural or regulatory mutation?

J Lab Clin Med. 1971 Dec;78(6):987.

Fabry's disease: evidence for a physically altered -galactosidase.法布里病：关于物理结构改变的α-半乳糖苷酶的证据。

Am J Hum Genet. 1972 May;24(3):256-66.

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Purification and properties of human alpha-galactosidases.人α-半乳糖苷酶的纯化及性质

J Biol Chem. 1972 Nov 25;247(22):7195-200.

On the existence and the enzymic interconversion of the isozymes of alpha-galactosidase in human organs.关于人体器官中α-半乳糖苷酶同工酶的存在及其酶促相互转化

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