Mitochondrial complex I activity is significantly decreased in a patient with maternally inherited type 2 diabetes mellitus and hypertrophic cardiomyopathy associated with mitochondrial DNA C3310T mutation: A cybrid study-Reference-Cited by-同舟云学术

Mitochondrial complex I activity is significantly decreased in a patient with maternally inherited type 2 diabetes mellitus and hypertrophic cardiomyopathy associated with mitochondrial DNA C3310T mutation: A cybrid study

Published:2006-11 Issue:2 Volume:74 Page:148-153
ISSN:0168-8227
Container-title:Diabetes Research and Clinical Practice
language:en
Short-container-title:Diabetes Research and Clinical Practice

Author:

Chen Jing,Hattori Yukiko,Nakajima Kazuo,Eizawa Takayuki,Ehara Takashi,Koyama Masamichi,Hirai Tetsuya,Fukuda Youji,Kinoshita Moritoshi,Sugiyama Atsushi,Hayashi Jun-Ichi,Onaya Toshimasa,Kobayashi Tetsuro,Tawata Masato

Publisher

Elsevier BV

Subject

Endocrinology,General Medicine,Endocrinology, Diabetes and Metabolism,Internal Medicine

Reference29 articles.

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3. Mitochondrial diabetes mellitus: a review;Gerbitz;Biochim. Biophys. Acta,1995

4. Maternally inherited diabetes and deafness: a new diabetes subtype;Maassen;Diabetologia,1996

5. Heteroplasmic mitochondrial DNA 3310 mutation in NADH dehydrogenase subunit 1 associated with type 2 diabetes, hypertrophic cardiomyopathy and mental retardation in a single patient;Hattori;Diabetes Care,2003

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