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Volumn 15, Issue 12, 2000, Pages 822-824

Mitochondrial DNA depletion in children

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA;

EID: 0034484855     PISSN: 08830738     EISSN: None     Source Type: Journal    
DOI: 10.1177/088307380001501213     Document Type: Article
Times cited : (17)

References (17)
  • 2
    • 0020557211 scopus 로고
    • Mitochondrial cytochrome deficiency presenting as a myopathy with hypotonia, external ophthalmoplegia, and lactic acidosis in an infant and as fatal hepatopathy in a second cousin
    • (1983) Ann Neurol , vol.14 , pp. 462-470
    • Boustany, R.N.1    Aprille, J.R.2    Halperin, J.3
  • 5
    • 0029086201 scopus 로고
    • Early onset encephalomyopathy associated with tissue-specific mitochondrial DNA depletion: A morphological, biochemical and molecular-genetic study
    • (1995) J Neurol , vol.242 , pp. 547-556
    • Marioti, C.1    Uziel, G.2    Carrara, F.3
  • 10
    • 4244015908 scopus 로고
    • Multifactorial congenital abnormallties-recurrent risks
    • Rudolph AM, Hoffman JIE (eds): Pediatrics Norwalk, CT/Los Altos, CA, Appleton & Lange
    • (1987) , pp. 364-366
    • Hall, B.D.1
  • 12
    • 0002082551 scopus 로고    scopus 로고
    • Mitochondrial encephalomyopathies
    • Rosenberg RN, Prusiner SB, DiMauro S, Barchi RL, Kunkel LM (eds): The Molecular and Genetic Basis of Neurological Diseases, 2nd ed. Boston, Butterworth-Heinemann
    • (1996) , pp. 665-694
    • DiMauro, S.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.