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Volumn 63, Issue 6, 1998, Pages 1594-1597

Getting to the nucleus of mitochondrial disorders: Identification of respiratory chain-enzyme genes causing Leigh syndrome

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL ENZYME;

EID: 0032471513     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/302169     Document Type: Editorial
Times cited : (84)

References (19)
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  • 5
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    • Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nulear-encoded mitochondrial metaloprotease
    • Casari G, De Fusco M, Ciarmatori S, Zeviani M, Mora M, Fernandez P, De Michele G, et al. (1998) Spastic paraplegia and OXPHOS impairment caused by mutations in paraplegin, a nulear-encoded mitochondrial metaloprotease. Cell 93:973-983
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    • The NuoI subunit of the Rhodobacter capsulatus respiratory complex I (equivalent to the bovine TYKY subunit) is required for proper assembly of the membraneous and peripheral domains of the enzyme
    • Chevallet M, Dupuis A, Lunardi J, van Belzen R, Albracht SP, Issartel JP (1997) The NuoI subunit of the Rhodobacter capsulatus respiratory complex I (equivalent to the bovine TYKY subunit) is required for proper assembly of the membraneous and peripheral domains of the enzyme. Eur J Biochem 250:451-458
    • (1997) Eur J Biochem , vol.250 , pp. 451-458
    • Chevallet, M.1    Dupuis, A.2    Lunardi, J.3    Van Belzen, R.4    Albracht, S.P.5    Issartel, J.P.6
  • 7
    • 0028986810 scopus 로고
    • Pyruvate dehydrogenase E1α deficiency: Males and females differ yet again
    • Dahl H-HM (1995) Pyruvate dehydrogenase E1α deficiency: males and females differ yet again. Am J Hum Genet 56: 553-557
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  • 8
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    • Genetic heterogeneity in Leigh syndrome
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    • Nuclear functions required for cytochrome c oxidase biogenesis in Saccharomyces cerevisiae
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    • (1992) Am J Hum Genet , vol.50 , pp. 852-858
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.