MtDNA Mutations in Maternally Inherited Diabetes: Presence of the 3397 ND1 Mutation Previously Associated with Alzheimer's and Parkinson's Disease-Reference-Cited by-同舟云学术

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MtDNA Mutations in Maternally Inherited Diabetes: Presence of the 3397 ND1 Mutation Previously Associated with Alzheimer's and Parkinson's Disease

Published:2004-04-22 Issue:1 Volume:135 Page:65-70
ISSN:0018-0661
Container-title:Hereditas
language:en
Short-container-title:

Author:

Cavelier Lucia,Erikson Inger,Tammi Martti,Jalonen Paula,Lindholm EVA,Jazin Elena,Smith Paul,Luthman Holger,Gyllensten Ulf

Publisher

Springer Science and Business Media LLC

Subject

Genetics,General Medicine

Reference23 articles.

1. Mitochondrial gene defects in patients with N1DDM;Alcolado;Diabetologia,1994

2. Maternally transmitted diabetes and deafness associated with a 10.4 kb mitochondrial DNA deletion;Ballinger;Nat. Genet.,1992

3. Phylogenetic analysis of Leber's hereditary optic neuropathy mitochondrial DNA's indicates multiple independent occurrences of the common mutations;Brown;Hum. Mutat.,1995

4. Leber's hereditary optic neuropathy: a model for mitochondrial neurodegenerative diseases;Brown;FASEB J.,1992

5. Mitochondrial DNA 3243 mutation is infrequent in Japanese diabetic patients with auditory disturbance;Fukunaga;Diabetes Care,1997

Cited by 18 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. Contribution of mitochondrial gene variants in diabetes and diabetic kidney disease;Frontiers in Endocrinology;2022-10-12

2. Whole mitochondrial genome sequencing of Malaysian patients with cardiomyopathy;PeerJ;2022-04-14

3. Mitochondrial Dysfunction in Parkinson’s Disease: Focus on Mitochondrial DNA;Biomedicines;2020-12-10

4. Mitochondrial ND1 T4216C and ND2 C5178A mutations are associated with maternally transmitted diabetes mellitus;Mitochondrial DNA Part A;2020-12-07

5. Neurological disorders and mitochondria;Molecular Aspects of Medicine;2020-02

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