The enigmatic relationship between mitochondrial dysfunction and Leber's hereditary optic neuropathy

被引：61

作者：

Brown, MD ^{[1
]}

机构：

[1] Emory Univ, Sch Med, Ctr Mol Med, Atlanta, GA 30322 USA

来源：

JOURNAL OF THE NEUROLOGICAL SCIENCES | 1999年 / 165卷 / 01期

关键词：

D O I：

10.1016/S0022-510X(99)00087-8

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：1 / 5

页数：5

共 26 条

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[4] BROWN MD, 1999, UNPUB OXIDATIVE PHOS
[5] Leber's hereditary optic neuropathy: Biochemical effect of 11778/ND4 and 3460/ND1 mutations and correlation with the mitochondrial genotype
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[J]. NEUROLOGY, 1997, 48 (06) : 1623 - 1632
[6] Functional consequences of the 3460-bp mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy
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[J]. JOURNAL OF THE NEUROLOGICAL SCIENCES, 1999, 165 (01) : 10 - 17
[7] COCK HR, 1995, AM J HUM GENET, V57, P1501
[8] The influence of nuclear background on the biochemical expression of 3460 Leber's hereditary optic neuropathy
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[J]. ANNALS OF NEUROLOGY, 1998, 44 (02) : 187 - 193
[9] FUNCTIONAL ALTERATIONS OF THE MITOCHONDRIALLY ENCODED ND4 SUBUNIT ASSOCIATED WITH LEBERS HEREDITARY OPTIC NEUROPATHY
ESPOSTI, MD
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[J]. FEBS LETTERS, 1994, 352 (03): : 375 - 379
[10] Respiration and growth defects in transmitochondrial cell lines carrying the 11778 mutation associated with Leber's hereditary optic neuropathy
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Johns, DR
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Chomyn, A
[J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (22) : 13155 - 13161

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