Mitochondrial DNA mutations are associated with both decreased insulin secretion and advanced microvascular complications in Japanese diabetic subjects

Journal of Diabetes and its Complications

Volumn 13, Issue 5-6, 1999, Pages 277-283

  Fukuda, Masataka ^a   Nakano, Shigeru ^a   Imaizumi, Noriko ^a   Kitazawa, Mitsutaka ^a   Nishizawa, Makoto ^a   Kigoshi, Toshikazu ^a   Uchida, Kenzo ^a  

^a KANAZAWA MEDICAL UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

C PEPTIDE; CREATININE; HEMOGLOBIN A1C; INSULIN; MITOCHONDRIAL DNA; ORAL ANTIDIABETIC AGENT; POTASSIUM ION; PROTEIN; SODIUM ION;

ADULT; AGED; ARTICLE; BASE PAIRING; CONTROLLED STUDY; DIABETES MELLITUS; DIABETIC MICROANGIOPATHY; DIABETIC NEPHROPATHY; DIABETIC NEUROPATHY; DIABETIC RETINOPATHY; FAMILY HISTORY; FEMALE; GENE MUTATION; GENETIC ANALYSIS; HUMAN; HUMAN EXPERIMENT; HYPERTENSION; INSULIN RELEASE; JAPAN; LEUKOCYTE; MAJOR CLINICAL STUDY; MALE; NORMAL HUMAN; POINT MUTATION; PRIORITY JOURNAL; PROTEINURIA; RESTRICTION FRAGMENT;

ADULT; AGED; AGED, 80 AND OVER; ASIAN CONTINENTAL ANCESTRY GROUP; BASE PAIRING; C-PEPTIDE; DIABETES MELLITUS, TYPE 1; DIABETES MELLITUS, TYPE 2; DIABETIC ANGIOPATHIES; DIABETIC NEUROPATHIES; DIABETIC RETINOPATHY; DNA PRIMERS; DNA, MITOCHONDRIAL; FEMALE; HUMANS; HYPERTENSION; INSULIN; JAPAN; MALE; MIDDLE AGED; POINT MUTATION; POLYMERASE CHAIN REACTION; REFERENCE VALUES; RESTRICTION MAPPING; RNA, TRANSFER, LEU;

EID: 0033549922     PISSN: 10568727     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1056-8727(99)00060-4     Document Type: Article

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