在日本家族性肌萎缩侧索硬化症中，超氧化物歧化酶1（SOD1）基因存在两个碱基对缺失时Cu/Zn超氧化物歧化酶（SOD1）活性的异常。 - Suppr

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超能文献

Abnormality of Cu/Zn superoxide dismutase (SOD1) activity in Japanese familial amyotrophic lateral sclerosis with two base pair deletion in the SOD1 gene.

作者信息

Nakashima K, Watanabe Y, Kuno N, Nanba E, Takahashi K

机构信息

Division of Neurology, Faculty of Medicine, Tottori University, Yonago, Japan.

出版信息

Neurology. 1995 May;45(5):1019-20. doi: 10.1212/wnl.45.5.1019-a.

DOI:10.1212/wnl.45.5.1019-a

PMID:7746377

Abstract

摘要

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Abnormality of Cu/Zn superoxide dismutase (SOD1) activity in Japanese familial amyotrophic lateral sclerosis with two base pair deletion in the SOD1 gene.在日本家族性肌萎缩侧索硬化症中，超氧化物歧化酶1（SOD1）基因存在两个碱基对缺失时Cu/Zn超氧化物歧化酶（SOD1）活性的异常。

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