Response to the letter to the editor regarding an article “Bilateral striatal necrosis caused by a founder mitochondrial 14459GA mutation in two independent Japanese families”

Kimitoshi Hirayanagi; Yoshio Ikeda

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Response to the letter to the editor regarding an article “Bilateral striatal necrosis caused by a founder mitochondrial 14459GA mutation in two independent Japanese families”

机译：对编辑函的回应有关一篇文章的“创始人线粒体14459g＆gt引起的双侧纹状体坏死;两个独立日本家庭的突变”

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来源
《Journal of the Neurological Sciences: Official Bulletin of the World Federation of Neurology》 |2017年第2017期|共2页
作者
Kimitoshi Hirayanagi; Yoshio Ikeda;
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作者单位

Department of Neurology Gunma University Graduate School of Medicine;

Department of Neurology Gunma University Graduate School of Medicine;

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原文格式 PDF
正文语种 eng
中图分类神经病学;
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外文文献

1. Response to the letter to the editor regarding an article “Bilateral striatal necrosis caused by a founder mitochondrial 14459GA mutation in two independent Japanese families” [J] . Kimitoshi Hirayanagi, Yoshio Ikeda Journal of the Neurological Sciences: Official Bulletin of the World Federation of Neurology . 2017,第期

机译：对编辑函的回应有关一篇文章的“创始人线粒体14459g＆gt引起的双侧纹状体坏死;两个独立日本家庭的突变”
2. Mitochondrial complex I NUBPL mutations cause combined dystonia with bilateral striatal necrosis and cerebellar atrophy [J] . B. Balint, G. Charlesworth, M. Stamelou, European journal of neurology: the official journal of the European Federation of Neurological Societies . 2019,第9期

机译：线粒体复合体I NUBPL突变导致组合肌剖性坏死和小脑萎缩
3. Mutations in the mitochondrial complex I assembly factor NDUFAF6 cause isolated bilateral striatal necrosis and progressive dystonia in childhood [J] . Baide-Mairena Heidy, Gaudo Paula, Marti-Sanchez Laura, Molecular genetics and metabolism . 2019,第3期

机译：线粒体复合体I组装因子Ndufaf6的突变导致童年时期的双侧双侧纹状体坏死和渐进性肌瘤
4. Mitochondrial complex I NUBPL mutations cause combined dystonia with bilateral striatal necrosis and cerebellar atrophy [O] . B. Balint, G. Charlesworth, M. Stamelou, -1

机译：线粒体复合体I NUBPL突变导致肌张力障碍合并双侧纹状体坏死和小脑萎缩
5. Bilateral striatal necrosis caused by a founder mitochondrial 14459G > A mutation in two independent Japanese families [O] . Kimitoshi Hirayanagi, Yuji Okamoto, Eriko Takai, 2017

机译：由创始人线粒体引起的双侧纹状体坏死14459g>两个独立日本家庭的突变

Response to the letter to the editor regarding an article “Bilateral striatal necrosis caused by a founder mitochondrial 14459GA mutation in two independent Japanese families”

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