Clinical features of diabetes mellitus with the mitochondrial DNA 3243 (A-G) mutation in Japanese: Maternal inheritance and mitochondria-related complications

Diabetes Research and Clinical Practice

Volumn 59, Issue 3, 2003, Pages 207-217

  Suzuki, Susumu ^a   Oka, Yoshitomo ^a   Kadowaki, Takashi ^b   Kanatsuka, Azuma ^c   Kuzuya, Takeshi ^d   Kobayashi, Masashi ^e   Sanke, Tokio ^f   Seino, Yutaka ^g   Nanjo, Kishio ^f,h  

^a TOHOKU UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

^b UNIVERSITY OF TOKYO   (Japan)

^c Kasori Hospital   (Japan)

^d Shioya General Hospital   (Japan)

^e UNIVERSITY OF TOYAMA   (Japan)

^f WAKAYAMA MEDICAL UNIVERSITY   (Japan)

^g KYOTO UNIVERSITY   (Japan)

^h Japan Stroke Society   (Japan)

Author keywords

Deafness; Diabetes mellitus; Diabetic nephropathy; Diabetic neuropathy; Diabetic retinopathy; Insulin; Mitochondrial DNA; Mitochondrial encephalomyopathy; Sick sinus syndrome; Wolff Parkinson White syndrome

Indexed keywords

INSULIN; MITOCHONDRIAL DNA;

ADULT; AGING; ARTICLE; BODY BUILD; CARDIOMYOPATHY; CASE FINDING; CLINICAL FEATURE; CONTROLLED STUDY; DEMENTIA; DEPRESSION; DIABETES MELLITUS; DIABETIC MICROANGIOPATHY; DIABETIC NEUROPATHY; DIABETIC RETINOPATHY; DISORDERS OF MITOCHONDRIAL FUNCTIONS; ENCEPHALOMYOPATHY; EXTRACHROMOSOMAL INHERITANCE; FEMALE; GENE MUTATION; GLUCOSE INTOLERANCE; HEARING IMPAIRMENT; HEART MUSCLE CONDUCTION DISTURBANCE; HUMAN; HUMAN CELL; INSULIN RELEASE; INSULIN TREATMENT; LEUKOCYTE; MAJOR CLINICAL STUDY; MALE; MATERNALLY INHERITED DIABETES MELLITUS AND DEAFNESS; MENTAL DEFICIENCY; NEUROMUSCULAR DISEASE; NEUROPSYCHIATRY; ONSET AGE; OPHTHALMOPLEGIA; PREVALENCE; RETINA MACULA DEGENERATION; SHORT STATURE; SICK SINUS SYNDROME; WOLFF PARKINSON WHITE SYNDROME;

ADULT; DEAFNESS; DIABETES MELLITUS, TYPE 1; DIABETES MELLITUS, TYPE 2; DIABETIC NEPHROPATHIES; DIABETIC NEUROPATHIES; DIABETIC RETINOPATHY; DNA, MITOCHONDRIAL; FEMALE; HUMANS; JAPAN; MALE; MIDDLE AGED; MITOCHONDRIAL ENCEPHALOMYOPATHIES; POINT MUTATION; PREVALENCE; SICK SINUS SYNDROME; WOLFF-PARKINSON-WHITE SYNDROME;

EID: 0037365908     PISSN: 01688227     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0168-8227(02)00246-2     Document Type: Article

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