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Volumn 49, Issue 2, 1997, Pages 598-600

A new mitochondrial DNA mutation associated with mitochondrial myopathy: tRNA(Leu)(UUR) 3254C-to-G

Author keywords

[No Author keywords available]

Indexed keywords

CYTOSINE; GUANINE; LEUCINE TRANSFER RNA; MITOCHONDRIAL DNA;

EID: 0030799693     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/WNL.49.2.598     Document Type: Article
Times cited : (35)

References (10)
  • 1
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    • Leu(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies
    • Leu(UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies. Nature 1990;348:651-653.
    • (1990) Nature , vol.348 , pp. 651-653
    • Goto, Y.1    Nonaka, I.2    Horai, S.3
  • 2
    • 0026004614 scopus 로고
    • A new mtDNA mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS)
    • Goto Y, Nonaka I, Horai S. A new mtDNA mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes (MELAS). Biochim Biophys Acta 1991;1097:238-240.
    • (1991) Biochim Biophys Acta , vol.1097 , pp. 238-240
    • Goto, Y.1    Nonaka, I.2    Horai, S.3
  • 5
    • 0025825012 scopus 로고
    • Strongly succinate dehydrogenase-reactive blood vessels in muscles from patients with mitochondrial myopathy, encephalopathy, lacticacidosis, and stroke-like episodes
    • Hasegawa H, Matsuoka T, Goto Y, Nonaka I. Strongly succinate dehydrogenase-reactive blood vessels in muscles from patients with mitochondrial myopathy, encephalopathy, lacticacidosis, and stroke-like episodes. Ann Neurol 1991;29:601-605.
    • (1991) Ann Neurol , vol.29 , pp. 601-605
    • Hasegawa, H.1    Matsuoka, T.2    Goto, Y.3    Nonaka, I.4
  • 6
    • 0019423856 scopus 로고
    • Sequence and organization of the human mitochondrial genome
    • Anderson S, Bankier AT, Barrell BG, et al. Sequence and organization of the human mitochondrial genome. Nature 1981;290:457-465.
    • (1981) Nature , vol.290 , pp. 457-465
    • Anderson, S.1    Bankier, A.T.2    Barrell, B.G.3
  • 7
    • 0029812866 scopus 로고    scopus 로고
    • Mitochondrial DNA and RNA processing in MELAS
    • Kaufmann P, Koga Y, Shanske S, et al. Mitochondrial DNA and RNA processing in MELAS. Ann Neurol 1996;40:172-180.
    • (1996) Ann Neurol , vol.40 , pp. 172-180
    • Kaufmann, P.1    Koga, Y.2    Shanske, S.3
  • 8
    • 0024365289 scopus 로고
    • Termination of transcription in human mitochondria: Identification and purification of a DNA binding protein factor that promotes termination
    • Kruse B, Narasimhan N, Attardi G. Termination of transcription in human mitochondria: identification and purification of a DNA binding protein factor that promotes termination. Cell 1989;58:391-397.
    • (1989) Cell , vol.58 , pp. 391-397
    • Kruse, B.1    Narasimhan, N.2    Attardi, G.3
  • 9
    • 0025863393 scopus 로고
    • Distinct clustering of point mutations in mitochondrial DNA among patients with mitochondrial encephalomyopathies and with Parkinson's disease
    • Ozawa T, Tanaka M, Ino H, et al. Distinct clustering of point mutations in mitochondrial DNA among patients with mitochondrial encephalomyopathies and with Parkinson's disease. Biochem Biophys Res Commun 1991;176:938-946.
    • (1991) Biochem Biophys Res Commun , vol.176 , pp. 938-946
    • Ozawa, T.1    Tanaka, M.2    Ino, H.3
  • 10
    • 0025371499 scopus 로고
    • Oxidative phosphorylation diseases. Disorders of two genomes
    • Shoffner JM, Wallace DC. Oxidative phosphorylation diseases. Disorders of two genomes. Adv Hum Genet 1990;19: 267-330.
    • (1990) Adv Hum Genet , vol.19 , pp. 267-330
    • Shoffner, J.M.1    Wallace, D.C.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.