Fatal hypertrophic cardiomyopathy associated with an A8296G mutation in the mitochondrial tRNA(Lys) gene.

Human mutation

Volumn 15, Issue 4, 2000, Pages 382-

  Akita, Y ^a   Koga, Y ^a   Iwanaga, R ^a   Wada, N ^a   Tsubone, J ^a   Fukuda, S ^a   Nakamura, Y ^a   Kato, H ^a  

^a KURUME UNIVERSITY SCHOOL OF MEDICINE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

AMINOACYL TRANSFER RNA; RNA; RNA, MITOCHONDRIAL; TRNA, LYSINE; TRNA, LYSINE-;

ARTICLE; CASE REPORT; DIZYGOTIC TWINS; FATALITY; FEMALE; GENETICS; HUMAN; HYPERTROPHIC CARDIOMYOPATHY; NEWBORN; POINT MUTATION; PREGNANCY; TWINS;

CARDIOMYOPATHY, HYPERTROPHIC; DISEASES IN TWINS; FATAL OUTCOME; FEMALE; HUMANS; INFANT, NEWBORN; POINT MUTATION; PREGNANCY; RNA; RNA, TRANSFER, AMINO ACYL; TWINS, DIZYGOTIC;

MLCS; MLOWN;

EID: 0034164636     PISSN: None     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/(sici)1098-1004(200004)15:4<382::aid-humu15>3.0.co;2-b     Document Type: Article

References (0)