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Volumn 129, Issue 3, 2008, Pages 441-443

Adult-onset hypertrophic cardiomyopathy manifested as initial major presentation of mitochondrial disease with A-to-G 3243 tRNA Leu(UUR) point mutation

Author keywords

Hypertrophic cardiomyopathy; Mitochondrial cardiomyopathy; Point mutation

Indexed keywords

CARNITINE; TRANSFER RNA; UBIDECARENONE; AMINOACYL TRANSFER RNA;

EID: 52949138204     PISSN: 01675273     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ijcard.2007.06.098     Document Type: Article
Times cited : (8)

References (6)
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  • 5
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    • Respiratory failure revealing mitochondrial myopathy in adults
    • Cros D., Palliyath S., DiMauro S., et al. Respiratory failure revealing mitochondrial myopathy in adults. Chest 101 (1992) 824-828
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  • 6
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    • Coexistence of mitochondrial DNA and beta myosin heavy chain mutations in hypertrophic cardiomyopathy with late congestive heart failure
    • Arbustini E., Fasani R., Morbini P., et al. Coexistence of mitochondrial DNA and beta myosin heavy chain mutations in hypertrophic cardiomyopathy with late congestive heart failure. Heart 80 (1998) 548-558
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.