A subtype of diabetes mellitus associated with a mutation in the mitochondrial gene-Reference-Cited by-同舟云学术

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A subtype of diabetes mellitus associated with a mutation in the mitochondrial gene

Published:1995 Issue:S14 Volume:18 Page:S137-S141
ISSN:0148-639X
Container-title:Muscle & Nerve
language:en
Short-container-title:Muscle Nerve

Author:

Kadowaki T.,Sakura H.,Otabe S.,Yasuda K.,Kadowaki H.,Mori Y.,Hagura R.,Akanuma Y.,Yazaki Y.

Publisher

Wiley

Subject

Physiology (medical),Cellular and Molecular Neuroscience,Clinical Neurology,Physiology

Reference11 articles.

1. Mutation in mitochondrial tRNALeu(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness

2. Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNA

3. Mitochondrial gene mutation and insulin-deficient type of diabetes mellitus

4. Glucokinase-defective NIDDM

5. Mitochondrial gene mutation in islet-cell-antibody-positive patients who were initially non-insulin-dependent diabetics

Cited by 9 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Pyrosequencing Is an Accurate and Reliable Method for the Analysis of Heteroplasmy of the A3243G Mutation in Patients with Mitochondrial Diabetes;The Journal of Molecular Diagnostics;2014-07

2. Mitochondrial Medicine;Emery and Rimoin's Principles and Practice of Medical Genetics;2013

3. The Clinical Variability of Maternally Inherited Diabetes and Deafness Is Associated with the Degree of Heteroplasmy in Blood Leukocytes;The Journal of Clinical Endocrinology & Metabolism;2009-08-01

4. Detection of Mutations in mtDNA;Mitochondria, 2nd Edition;2007

5. Progression of Cardiac Dysfunction in a Case of Mitochondrial Diabetes;Diabetes Care;2001-05-01

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