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Volumn 129, Issue 3, 2008, Pages 441-443
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Adult-onset hypertrophic cardiomyopathy manifested as initial major presentation of mitochondrial disease with A-to-G 3243 tRNA Leu(UUR) point mutation
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Author keywords
Hypertrophic cardiomyopathy; Mitochondrial cardiomyopathy; Point mutation
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Indexed keywords
CARNITINE;
TRANSFER RNA;
UBIDECARENONE;
AMINOACYL TRANSFER RNA;
ADULT;
ARTICLE;
CASE REPORT;
CLINICAL FEATURE;
DISEASE COURSE;
DISORDERS OF MITOCHONDRIAL FUNCTIONS;
GENE MUTATION;
GENETIC ANALYSIS;
HUMAN;
HYPERTROPHIC CARDIOMYOPATHY;
MALE;
PHYSICAL EXAMINATION;
PRIORITY JOURNAL;
CARDIOMYOPATHY, HYPERTROPHIC;
DIFFERENTIAL DIAGNOSIS;
GENETICS;
MITOCHONDRIAL DISEASES;
POINT MUTATION;
ADULT;
CARDIOMYOPATHY, HYPERTROPHIC;
DIAGNOSIS, DIFFERENTIAL;
HUMANS;
MALE;
MITOCHONDRIAL DISEASES;
POINT MUTATION;
RNA, TRANSFER, AMINO ACYL;
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EID: 52949138204
PISSN: 01675273
EISSN: None
Source Type: Journal
DOI: 10.1016/j.ijcard.2007.06.098 Document Type: Article |
Times cited : (8)
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References (6)
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