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Volumn 79, Issue 14, 2012, Pages 1517-1519

Revisiting the issue of mitochondrial dna contentinopticmitochondriopathies

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA;

EID: 84867566787     PISSN: 00283878     EISSN: 1526632X     Source Type: Journal    
DOI: 10.1212/WNL.0b013e31826d5f72     Document Type: Article
Times cited : (13)

References (7)
  • 2
    • 79551638162 scopus 로고    scopus 로고
    • Mitochondrial optic neuropathies: Disease mechanisms and therapeutic strategies
    • Yu-Wai-Man P, Griffiths PG, Chinnery PF. Mitochondrial optic neuropathies: Disease mechanisms and therapeutic strategies. Prog Retin Eye Res 2011;30:81-114.
    • (2011) Prog Retin Eye Res , vol.30 , pp. 81-114
    • Yu-Wai-Man, P.1    Griffiths, P.G.2    Chinnery, P.F.3
  • 3
    • 15244364005 scopus 로고    scopus 로고
    • Mitochondrial DNA content is decreased in autosomal dominant optic atrophy
    • Kim JY, Hwang JM, Ko HS, Seong MW, Park BJ, Park SS. Mitochondrial DNA content is decreased in autosomal dominant optic atrophy. Neurology 2005;64:966-972.
    • (2005) Neurology , vol.64 , pp. 966-972
    • Kim, J.Y.1    Hwang, J.M.2    Ko, H.S.3    Seong, M.W.4    Park, B.J.5    Park, S.S.6
  • 4
    • 0036724369 scopus 로고    scopus 로고
    • Increase of mitochondrial DNA in blood cells of patients of Leber's hereditary optic neuropathy with 11778 mutation
    • Yen MY, Chen CS, Wang AG, Wei YH. Increase of mitochondrial DNA in blood cells of patients of Leber's hereditary optic neuropathy with 11778 mutation. Br J Ophthalmol 2002;86:1027-1030.
    • (2002) Br J Ophthalmol , vol.86 , pp. 1027-1030
    • Yen, M.Y.1    Chen, C.S.2    Wang, A.G.3    Wei, Y.H.4
  • 5
    • 9144233107 scopus 로고    scopus 로고
    • The ND1 gene of complex I is a mutational hot spot for Leber's hereditary optic neuropathy
    • Valentino ML, Barboni P, Ghelli A, et al. The ND1 gene of complex I is a mutational hot spot for Leber's hereditary optic neuropathy. Ann Neurol 2004;56:631-641.
    • (2004) Ann Neurol , vol.56 , pp. 631-641
    • Valentino, M.L.1    Barboni, P.2    Ghelli, A.3
  • 6
    • 38849190029 scopus 로고    scopus 로고
    • OPA1 mutations associated with dominant optic atrophy impair oxidative phosphorylation and mitochondrial fusion
    • Zanna C, Ghelli A, Porcelli AM, et al. OPA1 mutations associated with dominant optic atrophy impair oxidative phosphorylation and mitochondrial fusion. Brain 2008;131:352-367.
    • (2008) Brain , vol.131 , pp. 352-367
    • Zanna, C.1    Ghelli, A.2    Porcelli, A.M.3
  • 7
    • 38849192448 scopus 로고    scopus 로고
    • OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes
    • Amati-Bonneau P, Valentino ML, Reynier P, et al. OPA1 mutations induce mitochondrial DNA instability and optic atrophy 'plus' phenotypes. Brain 2008;131:338-351.
    • (2008) Brain , vol.131 , pp. 338-351
    • Amati-Bonneau, P.1    Valentino, M.L.2    Reynier, P.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.