Maternally inherited diabetes and deafness (MIDD): A distinct subtype of diabetes associated with a mitochondrial tRNALeu(UUR) gene point mutation-Reference-Cited by-同舟云学术

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Maternally inherited diabetes and deafness (MIDD): A distinct subtype of diabetes associated with a mitochondrial tRNALeu(UUR) gene point mutation

Published:1995 Issue:S14 Volume:18 Page:S124-S130
ISSN:0148-639X
Container-title:Muscle & Nerve
language:en
Short-container-title:Muscle Nerve

Author:

van den Ouweland J. M. W.,Lemkes H. H. P. J.,Gerbitz K.-D.,Maassen J. A.

Publisher

Wiley

Subject

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

Reference43 articles.

1. Importance of maternal history of non-insulin dependent diabetic patients.

2. Mitochondrial gene defects in patients with NIDDM

3. Sequence and organization of the human mitochondrial genome

4. Japanese case of diabetes mellitus and . deafness with mutation in mitochondrial tRNALeu(UUR)gene

5. Mitochondrial diabetes revisited

Cited by 32 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. The genomic mosaic of mitochondrial dysfunction: Decoding nuclear and mitochondrial epigenetic contributions to maternally inherited diabetes and deafness pathogenesis;Heliyon;2024-07

2. Diabetes mellitus and hearing loss: A review;Ageing Research Reviews;2021-11

3. Mapping and editing animal mitochondrial genomes: can we overcome the challenges?;Philosophical Transactions of the Royal Society B: Biological Sciences;2019-12-02

4. Mitochondrial DNA associations with East Asian metabolic syndrome;Biochimica et Biophysica Acta (BBA) - Bioenergetics;2018-09

5. Clinically Focused Molecular Investigation of 1000 Consecutive Families with Inherited Retinal Disease;Ophthalmology;2017-09

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