Lipoma and opthalmoplegia in mitochondrial diabetes associated with small heteroplasmy level of 3243 tRNALeu(UUR) mutation

Diabetes Research and Clinical Practice

Volumn 63, Issue 3, 2004, Pages 225-229

  Suzuki, Yoshihiko ^a,b,c,e   Nishimaki, K ^b   Taniyama, M ^c   Muramatsu, T ^d   Atsumi, Y ^a   Matsuoka, K ^a   Ohta, S ^b  

^a SAISEIKAI CENTRAL HOSPITAL   (Japan)

^b Graduate School of Medicine   (Japan)

^c SHOWA UNIVERSITY FUJIGAOKA HOSPITAL   (Japan)

^d KEIO UNIVERSITY   (Japan)

^e Hoken Dohjin Medical Foundation   (Japan)

Author keywords

3243 mitochondrial DNA mutation; Lipoma; Mitochondrial diabetes; Oculomotor palsy

Indexed keywords

CYTOCHROME C OXIDASE; M PROTEIN; MESSENGER RNA; POLYPEPTIDE; TRANSFER RNA; URIDINE DERIVATIVE;

AGED; ANTICODON; ARTICLE; AUTOIMMUNE DISEASE; CASE REPORT; CODON; DIABETES MELLITUS; DIPLOPIA; DISEASE ASSOCIATION; DISORDERS OF MITOCHONDRIAL FUNCTIONS; ENZYME DEFICIENCY; GENE MUTATION; HETEROPLASMY; HISTOPATHOLOGY; HUMAN; LIPOMA; MALE; MONONEUROPATHY; OPHTHALMOPLEGIA; PARALYSIS; PATHOGENESIS; TARGET ORGAN;

EID: 0942300610     PISSN: 01688227     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.diabres.2003.10.024     Document Type: Letter

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