A5814G mutation in mitochondrial DNA can cause mitochondrial myopathy and cardiomyopathy

Journal of Child Neurology

Volumn 16, Issue 7, 2001, Pages 531-533

  Karadimas, C ^a   Tanji, K ^a   Geremek, M ^a   Chronopoulou, P ^a   Vu, T ^a   Krishna, S ^a   Sue, C M ^a   Shanske, S ^a   Bonilla, E ^a   DiMauro, S ^a  

^a The New York Presbyterian Hospital   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADENINE; CYSTEINE; GUANINE; MITOCHONDRIAL DNA; TRANSFER RNA;

ARTICLE; BLOOD; CARDIOMYOPATHY; CASE REPORT; CHILDHOOD; CONTROLLED STUDY; DIFFERENTIAL DIAGNOSIS; DNA DETERMINATION; FIBROBLAST; GENE MUTATION; GENETIC HETEROGENEITY; HUMAN; HYPERTROPHIC CARDIOMYOPATHY; LACTIC ACIDOSIS; MALE; MITOCHONDRIAL MYOPATHY; MUSCLE; POINT MUTATION; PRESCHOOL CHILD; PRIORITY JOURNAL;

EID: 0034910767     PISSN: 08830738     EISSN: None     Source Type: Journal    
DOI: 10.1177/088307380101600715     Document Type: Article

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