Maternally inherited hypertrophic cardiomyopathy: A manifestation of mitochondrial DNA mutations - Clinical course in two families

Pediatric Cardiology

Volumn 22, Issue 1, 2001, Pages 14-22

  Dipchand, A I ^a   Tein, I ^a   Robinson, B ^a   Benson, L N ^a  

^a HOSPITAL FOR SICK CHILDREN   (Canada)

Author keywords

Hypertrophic cardiomyopathy; Mitochondrial tRNA point mutation

Indexed keywords

MITOCHONDRIAL DNA; TRANSFER RNA;

ARTICLE; BLOOD CHEMISTRY; BRAIN DISEASE; CARDIOMYOPATHY; CLINICAL FEATURE; DISEASE COURSE; ECHOCARDIOGRAPHY; ELECTROCARDIOGRAM; EXTRACHROMOSOMAL INHERITANCE; FAMILY; GENETIC ANALYSIS; HEARING LOSS; HEART CATHETERIZATION; HEMODYNAMICS; HUMAN; HYPERTROPHIC CARDIOMYOPATHY; MULTIPLE ORGAN FAILURE; MYOPATHY; PEDIGREE; POINT MUTATION; STROKE; SUDDEN DEATH;

ADOLESCENT; ADULT; AGED; CARDIOMYOPATHY, HYPERTROPHIC; CHILD; CHILD, PRESCHOOL; DNA MUTATIONAL ANALYSIS; DNA, MITOCHONDRIAL; ECHOCARDIOGRAPHY; ELECTROCARDIOGRAPHY; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HEART FAILURE, CONGESTIVE; HUMANS; INFANT; INFANT, NEWBORN; MALE; MIDDLE AGED; MITOCHONDRIAL MYOPATHIES; POINT MUTATION; RETROSPECTIVE STUDIES; RNA, TRANSFER, ILE; SEX CHROMOSOME ABERRATIONS; X CHROMOSOME;

EID: 0035126619     PISSN: 01720643     EISSN: None     Source Type: Journal    
DOI: 10.1007/s002460010145     Document Type: Article

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