A point mutation in the mitochondrial tRNALeu(UUR) gene in melas (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes)

Biochemical and Biophysical Research Communications

Volumn 173, Issue 3, 1990, Pages 816-822

  Kobayashi, Yoko ^a,b   Momoi, Mariko Y ^a,b   Tominaga, Kaoru ^a,b   Momoi, Takashi ^a,b   Nihei, Kenji ^b,c   Yanagisawa, Masayoshi ^a,b   Kagawa, Yasuo ^a,b   Ohta, Shigeo ^a,b  

^a JICHI MEDICAL UNIVERSITY   (Japan)

^b NATIONAL INSTITUTE OF MENTAL HEALTH   (Japan)

^c NATIONAL CHILDREN S HOSPITAL   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

ENDOGENOUS COMPOUND; MITOCHONDRIAL DNA; TRANSFER RNA;

ARTICLE; BRAIN DISEASE; CLINICAL ARTICLE; CONTROLLED STUDY; DISORDERS OF MITOCHONDRIAL FUNCTIONS; DNA SEQUENCE; HUMAN; HUMAN CELL; LACTIC ACIDOSIS; MITOCHONDRIAL MYOPATHY; POINT MUTATION; PRIORITY JOURNAL; RNA GENE; STROKE;

ACIDOSIS, LACTIC; BASE SEQUENCE; BRAIN DISEASES; CASE REPORT; CELL LINE; CEREBROVASCULAR DISORDERS; CHILD; DNA, MITOCHONDRIAL; FEMALE; HUMAN; MITOCHONDRIA; MOLECULAR SEQUENCE DATA; MUTATION; NUCLEIC ACID CONFORMATION; RNA, TRANSFER, LEU; SUPPORT, NON-U.S. GOV'T;

EID: 0025534162     PISSN: 0006291X     EISSN: 10902104     Source Type: Journal    
DOI: 10.1016/S0006-291X(05)80860-5     Document Type: Article

References (30)

1. Compilation of tRNA sequences and sequences of tRNA genes