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Volumn 336, Issue 4, 2005, Pages 1003-1004

Commentary to mitDNA research for the pathogenesis of mitochondrial disorders

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA; RIBOSOME RNA; TRANSFER RNA;

EID: 25644454256     PISSN: 0006291X     EISSN: 10902104     Source Type: Journal    
DOI: 10.1016/j.bbrc.2005.07.121     Document Type: Short Survey
Times cited : (2)

References (11)
  • 2
    • 4744356235 scopus 로고    scopus 로고
    • Sequence analysis of the complete mitochondrial genome in patients with mitochondrial encephaloneuromyopathies lacking the common pathogenic DNA mutations
    • P. Da Pozzo, E. Cardaioli, E. Radi, and A. Federico Sequence analysis of the complete mitochondrial genome in patients with mitochondrial encephaloneuromyopathies lacking the common pathogenic DNA mutations Biochem. Biophys Res. Commun. 324 2004 360 364
    • (2004) Biochem. Biophys Res. Commun. , vol.324 , pp. 360-364
    • Da Pozzo, P.1    Cardaioli, E.2    Radi, E.3    Federico, A.4
  • 3
    • 0033981680 scopus 로고    scopus 로고
    • Mitochondrial defects in cardiomyopathy and neuromuscular disease
    • D.C. Wallace Mitochondrial defects in cardiomyopathy and neuromuscular disease Am. Heart J. 139 2000 S70 S85
    • (2000) Am. Heart J. , vol.139
    • Wallace, D.C.1
  • 5
    • 0036069847 scopus 로고    scopus 로고
    • Sequence analysis of the complete mitochondrial genome in patients with Leber's hereditary optic neuropathy lacking the three most common pathogenic DNA mutations
    • S. Fauser, J. Luberichs, D. Besch, and B. Leo-Kottler Sequence analysis of the complete mitochondrial genome in patients with Leber's hereditary optic neuropathy lacking the three most common pathogenic DNA mutations Biochem. Biophys. Res. Commun. 295 2002 342 347
    • (2002) Biochem. Biophys. Res. Commun. , vol.295 , pp. 342-347
    • Fauser, S.1    Luberichs, J.2    Besch, D.3    Leo-Kottler, B.4
  • 6
    • 0347721039 scopus 로고    scopus 로고
    • A novel sporadic mutation in cytochrome c oxidase subunit II as a cause of rhabdomyolysis
    • R. McFarland, R.W. Taylor, P.F. Chinnery, N. Howell, and D.M. Turnbull A novel sporadic mutation in cytochrome c oxidase subunit II as a cause of rhabdomyolysis Neuromuscul. Disord. 14 2004 162 166
    • (2004) Neuromuscul. Disord. , vol.14 , pp. 162-166
    • McFarland, R.1    Taylor, R.W.2    Chinnery, P.F.3    Howell, N.4    Turnbull, D.M.5
  • 11
    • 0033659832 scopus 로고    scopus 로고
    • A novel homoplasmic mutation in mtDNA with a single evolutionary origin as a risk factor for cardiomyopathy
    • W.S. Shin, M. Tanaka, J. Suzuki, C. Hemmi, and T. Toyo-oka A novel homoplasmic mutation in mtDNA with a single evolutionary origin as a risk factor for cardiomyopathy Am. J. Hum. Genet. 67 2000 1617 1620
    • (2000) Am. J. Hum. Genet. , vol.67 , pp. 1617-1620
    • Shin, W.S.1    Tanaka, M.2    Suzuki, J.3    Hemmi, C.4    Toyo-Oka, T.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.