A novel mutation in the mitochondrial tRNA(Thr) gene associated with a mitochondrial encephalomyopathy

Biochemical and Biophysical Research Communications

Volumn 225, Issue 1, 1996, Pages 180-185

  Nishino, Ichizo ^a   Seki, Ayumi ^c   Maegaki, Yoshihiro ^c   Takeshita, Kenzo ^c   Horai, Satoshi ^d   Nonaka, Ikuya ^b   Goto, Yu Ichi ^a  

^a NATIONAL INSTITUTE OF NEUROSCIENCE   (Japan)

^b NATIONAL INSTITUTE OF MENTAL HEALTH   (Japan)

^c TOTTORI UNIVERSITY HOSPITAL   (Japan)

^d NATIONAL INSTITUTE OF GENETICS   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

CYTOCHROME B; CYTOCHROME C OXIDASE; MITOCHONDRIAL DNA; THREONINE TRANSFER RNA;

ADOLESCENT; ARTICLE; BLOOD; CASE REPORT; CONTROLLED STUDY; DNA POLYMORPHISM; DNA SEQUENCE; ENCEPHALOMYOPATHY; ENZYME DEFICIENCY; HEARING LOSS; HUMAN; HUMAN TISSUE; MALE; MENTAL DEFICIENCY; MISSENSE MUTATION; MUSCLE; MUSCLE BIOPSY; MUSCLE WEAKNESS; NUCLEIC ACID BASE SUBSTITUTION; POINT MUTATION; PRIORITY JOURNAL; RNA GENE; SEIZURE; SKIN FIBROBLAST;

EID: 0030570779     PISSN: 0006291X     EISSN: None     Source Type: Journal    
DOI: 10.1006/bbrc.1996.1150     Document Type: Article

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