A Japanese family with mutation in the proteinase inhibitor 12 L47P gene: A case report

被引：5

作者：

Amano-Takeshige, Haruka ^{[1
]}

Oyama, Genko ^{[1
]}

Kanai, Kazuaki ^{[1
]}

Miyagawa, Toji ^{[2
]}

Mitsui, Jun ^{[2
]}

Ugawa, Yoshikazu ^{[3
]}

Tsuji, Shoji ^{[2
]}

Hattori, Nobutaka ^{[1
]}

机构：

[1] Juntendo Univ, Dept Neurol, Fac Med, Tokyo, Japan

[2] Univ Tokyo, Dept Neurol, Tokyo, Japan

[3] Fukushima Univ, Dept Neurol, Fukushima, Japan

来源：

JOURNAL OF THE NEUROLOGICAL SCIENCES | 2018年 / 384卷

基金：

日本学术振兴会;

关键词：

Neuroserpin; Familial encephalopathy with neuroserpin; inclusion bodies; Progressive myoclonus epilepsy; L47P mutation; PROGRESSIVE MYOCLONUS EPILEPSY; NEUROSERPIN INCLUSION-BODIES; ENCEPHALOPATHY; DEMENTIA; NEURONS;

D O I：

10.1016/j.jns.2017.11.029

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

引用

页码：126 / 128

页数：3

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