Comparison of Clinical Pictures of Mitochon-drial Encephalomyopathy with tRNALeu(UUR) Mutation in 3243 with that in 3254

Brain and Nerve

Volumn 50, Issue 12, 1998, Pages 1089-1092

  Mitsuoka, Takako ^a   Kawarai, Toshitaka ^a   Watanabe, Chigusa ^a   Katayama, Sadao ^a   Nakamura, Shigenobu ^a  

^a HIROSHIMA UNIV SCHOOL OF MEDICINE   (Japan)

Author keywords

CPEO; MELAS; Mitochondria DNA; Mitochondrial encephalomyopathy; TRNAleu(ucr) point mutation

Indexed keywords

MITOCHONDRIAL DNA; NUCLEOTIDE; TRANSFER RNA;

ADULT; ARTICLE; CASE REPORT; ENCEPHALOMYOPATHY; HUMAN; HUMAN TISSUE; MALE; MUSCLE ATROPHY; MUSCLE BIOPSY; PHENOTYPE; POINT MUTATION;

EID: 0032458587     PISSN: 00068969     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (8)

1. LeuUUUR) 254 G- to -G. Neurology 49 : 598-600, 1997
2. Chwen-Yi Yang, Hing-Chung Lam, et al : MELAS syndrome associated with diabetes mellitus and hyperthyroidism : A case report from Taiwan. Clin Endocrinol 43: 235-239, 1995
3. Leu(UUA)GI32431 mutation: Clinical study. Brain 118: 721-734, 1995
4. Mariotti C, Savarese N, et al : Genotype to phenotype correlations in mitochondrial encephalomyopathies associated with the A3243G mutation of mitochondrial DNA. J Neurol 242 : 304-312, 1995