Mitochondrial DNA analysis in the Turkish Leber's hereditary optic neuropathy population

被引：0
作者：
C F Dogulu
T Kansu
V Seyrantepe
M Ozguc
H Topaloglu
D R Johns
机构：
[1] Institute of Neurological Sciences and Psychiatry,Department of Neurology
[2] Neuro-Ophthalmology Unit Hacettepe University,Department of Medical Biology
[3] Hacettepe University Faculty of Medicine,undefined
[4] Department of Neurology,undefined
[5] Pediatric Neurology Division Hacettepe University Hospitals,undefined
[6] Department of Neurology,undefined
[7] Neuromuscular Disease Division Beth Israel Hospital Harvard Medical School,undefined
来源：
Eye | 2001年 / 15卷
关键词：
LHON; mtDNA; mtDNA mutations;
D O I：
暂无
中图分类号：
学科分类号：
摘要：
Purpose To define the prevalence of a panel of mitochondrial DNA (mtDNA) mutations associated with Leber's hereditary optic neuropathy (LHON) in the Turkish LHON population. LHON-associated mtDNA mutations have been found in LHON patients from around the world, but the Turkish LHON population has not been studied.
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页码：183 / 188
页数：5
相关论文
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