Brain stem lesion in mitochondrial DNA G11778A mutation of Leber's hereditary optic neuropathy

被引：0
|
作者：
Chen, Yan-Ting [1 ,2 ]
Chen, Wei-Liang [3 ]
Chen, San-Ni [1 ]
Liu, Chin-San [4 ,5 ,6 ]
机构：
[1] Changhua Christian Hosp, Dept Ophthalmol, Changhua 500, Taiwan
[2] Natl Yang Ming Univ, Inst Clin Med, Taipei 112, Taiwan
[3] Changhua Christian Hosp, Dept Med Imaging, Changhua 500, Taiwan
[4] Changhua Christian Hosp, Vasc & Genom Ctr, Changhua 500, Taiwan
[5] Changhua Christian Hosp, Dept Neurol, Changhua 500, Taiwan
[6] China Med Univ, Coll Chinese Med, Grad Inst Integrated Med, Taichung, Taiwan
来源：
JOURNAL OF THE FORMOSAN MEDICAL ASSOCIATION | 2015年 / 114卷 / 07期
关键词：
D O I：
10.1016/j.jfma.2014.01.005
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
[No abstract available]
引用
收藏
页码：668 / 669
页数：2
相关论文
共 50 条
  • [1] Clinical phenotype and the G11778A mutation of mitochondrial DNA in patients with Leber's hereditary optic neuropathy in Taiwan
    Chu, CC
    Huang, CC
    Kao, LY
    Kuo, HC
    Yu, TN
    Tso, DJ
    Lee, HC
    Wei, YH
    [J]. NEURO-OPHTHALMOLOGY, 2001, 26 (04) : 207 - 216
  • [2] A double mutation (G11778A and G12192A) in mitochondrial DNA associated with Leber's hereditary optic neuropathy and cardiomyopathy
    Mimaki, M
    Ikota, A
    Sato, A
    Komaki, H
    Akanuma, J
    Nonaka, I
    Goto, Y
    [J]. JOURNAL OF HUMAN GENETICS, 2003, 48 (01) : 47 - 50
  • [3] A double mutation (G11778A and G12192A) in mitochondrial DNA associated with Leber's hereditary optic neuropathy and cardiomyopathy
    M. Mimaki
    A. Ikota
    A. Sato
    H. Komaki
    J. Akanuma
    I. Nonaka
    Y. Goto
    [J]. Journal of Human Genetics, 2003, 48 : 47 - 50
  • [4] Leber hereditary optic neuropathy: Does heteroplasmy influence the inheritance and expression of the G11778A mitochondrial DNA mutation?
    Chinnery, PF
    Andrews, RM
    Turnbull, DM
    Howell, N
    [J]. AMERICAN JOURNAL OF MEDICAL GENETICS, 2001, 98 (03): : 235 - 243
  • [5] Leber's Hereditary Optic Neuropathy with Mitochondrial DNA Mutation G11778A: A Systematic Literature Review and Meta-Analysis
    Yuan, Jiajia
    Zhao, Jiaxun
    Ye, Chong
    Pang, Long
    Zhang, Xin
    Luk, Alvin
    Du, Yangyang
    Fan, Kai Yoon
    Zhang, Xiaowen
    Li, Bin
    Chen, Changzheng
    [J]. BIOMED RESEARCH INTERNATIONAL, 2023, 2023
  • [6] Hereditary cerebellar ataxia with Leber's hereditary optic neuropathy mitochondrial DNA 11778 mutation
    Murakami, T
    Mita, S
    Tokunaga, M
    Maeda, H
    Ueyama, H
    Kumamoto, T
    Uchino, M
    Ando, M
    [J]. JOURNAL OF THE NEUROLOGICAL SCIENCES, 1996, 142 (1-2) : 111 - 113
  • [7] Mitochondrial DNA haplogroup distribution in pedigrees of Southeast Asian G11778A Leber hereditary optic neuropathy
    Tharaphan, Pattamon
    Chuenkongkaew, Wanicha L.
    Luangtrakool, Konion
    Sanpachudayan, Thitima
    Suktitipat, Bhooni
    Suphavilai, Rungnapa
    Srisawat, Chatchawan
    Sura, Thanyachai
    Lertrit, Patcharee
    [J]. JOURNAL OF NEURO-OPHTHALMOLOGY, 2006, 26 (04) : 264 - 267
  • [8] Phylogenetic assessment of the mitochondrial DNA displacement loop haplotype in Japanese patients with Leber's hereditary optic neuropathy harboring the mitochondrial DNA G11778A mutation
    Isashiki, Y
    Sonoda, S
    Izumo, S
    Sakamoto, T
    Tachikui, H
    Inoue, I
    [J]. OPHTHALMIC RESEARCH, 2003, 35 (04) : 224 - 231
  • [9] mtDNA haplogroup distribution in Chinese patients with Leber's hereditary optic neuropathy and G11778A mutation
    Ji, Yanli
    Jia, Xiaoyun
    Zhang, Qingjiong
    Yao, Yong-Gang
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2007, 364 (02) : 238 - 242
  • [10] Only male matrilineal relatives with Leber's hereditary optic neuropathy in a large Chinese family carrying the mitochondrial DNA G11778A mutation
    Qu, J
    Li, RH
    Tong, Y
    Hu, YW
    Zhou, XT
    Qian, YP
    Lu, F
    Guan, MX
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2005, 328 (04) : 1139 - 1145
12345