A case of adult-onset mitochondrial encephalopathy due to m.4296G>A gene abnormality-Reference-Cited by-同舟云学术

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A case of adult-onset mitochondrial encephalopathy due to m.4296G>A gene abnormality

Published:2019 Issue:10 Volume:59 Page:636-640
ISSN:0009-918X
Container-title:Rinsho Shinkeigaku
language:en
Short-container-title:Rinsho Shinkeigaku

Author:

Takahashi Kai¹,Yamahara Kanako¹,Ito Kouhei²,Iwaoka Kazuhiro¹,Goto Yuichi³,Terayama Yasuo¹

Affiliation:

1. Department of Neurology and Gerontology, Iwate Medical University

2. Department of Internal Medicine, Hachinohe Red Cross Hospital

3. Department of Ultrastructural Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry

Publisher

Societas Neurologica Japonica

Subject

Clinical Neurology

Link

https://www.jstage.jst.go.jp/article/clinicalneurol/59/10/59_cn-001292/_pdf

Reference11 articles.

1. 1) DiMauro S, Hirana M, Schon EA, editors. Mitochondrial medicine. London: Informa Healthcare; 2006. p. 7-26.

2. 2) Rahman S, Blok RB, Dahl HH, et al. Leigh syndrome: clinical features and biochemical and DNA abnormalities. Ann Neurol 1996;39:343-351.

3. 3) Dahl H. Getting to the nucleus of mitochondrial disorders: identification of respiratory chain-enzyme genes causing Leigh syndrome. Am J Hum Genet 1998;63:1594-1597.

4. 4) Finsterer J. Leigh and Leigh-like syndrome in children and adults. Pediatric Neurology 2008;39:223-235.

5. 5) Lee JS, Kim H, Lim BC, et al. Leigh syndrome in childhood: neurologic progression and functional outcome. Clinical Neurology 2016;12:181-187.

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